Table of Contents

 

UNITED STATES SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D. C. 20549

FORM 10-QSB

 

[ x ] Quarterly report under Section 13 or 15(d) of the Securities Exchange Act of 1934

For the quarterly period ended March 31, 2006 or

 

[

] Transition report under Section 13 or 15(d) of the Securities Exchange Act of 1934

For the transition period from ______ to ______

 

1-9731

(Commission file No.)

 

ARRHYTHMIA RESEARCH TECHNOLOGY, INC.

(Exact name of small business issuer as specified in its charter)

 

DELAWARE

72-0925679

(State or other jurisdiction of incorporation or organization)

(I.R.S. employer identification no.)

 

25 Sawyer Passway

Fitchburg, Massachusetts 01420

(Address of principal executive offices)

 

(978) 345-5000

(Issuer's telephone number, including area code)

 

 

 

Check whether the issuer (1) filed all reports required to be filed by Section 13 or 15(d) of the Exchange Act during the past 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes X No___.

 

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes _ No X

As of May 5, 2006 there were 2,666,194 shares of the Company’s common stock outstanding.

 

Transitional Small Business Disclosure Format

Yes

No

X

 

 

 

 

ARRHYTHMIA RESEARCH TECHNOLOGY, INC.

TABLE OF CONTENTS

FORM 10-QSB

March 31, 2006

PART I - FINANCIAL INFORMATION 1
     Item 1. Consolidated Financial Statements 1
         Consolidated Balance Sheets 1
         Consolidated Statements of Income 2
         Consolidated Statements of Cash Flows 3
         Notes to the Consolidated Financial Statements 4
     Item 2. Management's Discussion and Analysis of Financial Condition and Results of Operations 6
     Item 3. Controls and Procedures 9
PART II - OTHER INFORMATION 10
    Item 6. Exhibits 10
    SIGNATURES 10
 
Exhibit 31.1 - Certification of Chief Executive Officer pursuant to section 302 of the Sarbanes-Oxley Act of 2002 X-1
Exhibit 31.2 - Certification of Chief Financial Officer pursuant to section 302
of the Sarbanes-Oxley Act of 2002
X-2
Exhibit 32.1 - Certification of Chief Executive Officer pursuant to section 906
of the Sarbanes-Oxley Act of 2002
X-3
Exhibit 32.2 - Certification of Chief Financial Officer pursuant to section 906
of the Sarbanes-Oxley Act of 2002
X-4

 

 

i

 

 

 

PART I - FINANCIAL INFORMATION

Item 1. Consolidated Financial Statements

 

ARRHYTHMIA RESEARCH TECHNOLOGY, INC. AND SUBSIDIARY

Consolidated Balance Sheets

(Unaudited)

ASSETS

March 31,
2006

 

December 31,
2005

Current assets:

 

 

 

 

 

Cash and cash equivalents

$

1,875,994

 

$

1,931,823

Trade and other accounts receivable, net of allowance for

    doubtful accounts of $18,600

 

3,053,733

 

 

2,069,551

Inventories, net

 

1,825,658

 

 

1,732,356

Deferred income taxes, net

 

94,500

 

 

113,000

Deposits, prepaid expenses and other current assets

 

285,677

 

 

343,200

   Total current assets

 

7,135,562

 

 

6,189,930

 

 

 

 

 

 

Property and equipment, net of accumulated depreciation of

$6,265,068 and $6,077,672

 

4,851,377

 

 

4,695,946

Goodwill

 

1,479,727

 

 

1,479,727

Other intangible assets, net

 

209,046

 

 

225,383

Deferred income taxes, net

 

67,000

 

 

67,000

Other assets

 

103,551

 

 

162,662

Total assets

$

13,846,263

 

$

12,820,648

 

 

 

 

 

 

LIABILITIES AND SHAREHOLDERS’ EQUITY

 

 

 

 

 

 

 

 

 

 

 

Current liabilities:

 

 

 

 

 

Accounts payable

$

942,363

 

$

490,774

Accrued expenses

 

361,518

 

 

312,257

   Total current liabilities

 

1,303,881

 

 

803,031

 

 

 

 

 

 

Shareholders’ equity:

 

 

 

 

 

Preferred stock, $1 par value; 2,000,000 shares authorized,

       none issued

 

-

 

 

-

Common stock, $0.01 par value; 10,000,000 shares authorized,

       3,926,491 shares issued

 

39,265

 

 

39,265

Additional paid-in-capital

 

9,735,228

 

 

9,731,469

Common stock held in treasury, 1,260,297 shares at cost

 

(3,451,120)

 

 

(3,451,120)

Retained earnings

 

6,219,009

 

 

5,698,003

   Total shareholders’ equity

 

12,542,382

 

 

12,017,617

   Total liabilities and shareholders’ equity

$

13,846,263

 

$

12,820,648

 

 

 

 

 

 

 

The accompanying notes are an integral part of the consolidated financial statements.

 

1

 

 

ARRHYTHMIA RESEARCH TECHNOLOGY, INC. AND SUBSIDIARY

Consolidated Statements of Income

(Unaudited)

 

 

Three Months Ended

March 31,

 

2006

2005

Revenue

$

4,269,047

$

3,107,699

Cost of sales

 

2,903,267

 

1,942,918

Gross profit

 

1,365,780

 

1,164,781

Selling and marketing

 

142,455

 

160,858

General and administrative

 

385,976

 

331,755

Research and development

 

17,456

 

16,961

Income from operations

 

819,893

 

655,207

Other income (expense), net

 

(14,887)

 

6,497

Income before income taxes

 

805,006

 

661,704

Income tax provision

 

284,000

 

233,000

Net income

$

521,006

$

428,704

Net income per share – basic

$

0.20

$

0.16

Net income per share – diluted

$

0.19

$

0.16

Cash dividends declared per share

$

-

$

0.06

Weighted average common shares

outstanding – basic

 

2,666,194

 

2,663,945

Weighted average common shares

outstanding – diluted

 

2,696,416

 

2,696,686

 

The accompanying notes are an integral part of the consolidated financial statements.

 

2

 

 

 

ARRHYTHMIA RESEARCH TECHNOLOGY, INC. AND SUBSIDIARY

Consolidated Statements of Cash Flows

(Unaudited)

 

Three Months Ended
March 31,

 

 

2006

2005

 

Cash flows from operating activities:

 

 

 

 

 

 

Net income

$

521,006 

$

428,704 

 

Adjustments to reconcile net income to net cash provided by

(used in) operating activities:

 

 

 

 

 

Depreciation and amortization

 

204,330 

 

168,280 

 

Share based compensation

 

3,759 

 

 

Changes in operating assets and liabilities:

 

 

 

 

 

    Trade and other accounts receivable

 

(984,182)

 

(307,832)

 

    Inventories

 

(93,302)

 

(99,205)

 

    Deposits, prepaid expenses and other assets

 

135,101 

 

(146,742)

 

    Accounts payable and accrued expenses

 

500,850 

 

(116,687)

 

        Net cash provided by (used in) operating activities

 

287,562 

 

(73,482)

 

Cash flows from investing activities:

 

 

 

 

 

Capital expenditures, net of disposals

 

(343,391)

 

(214,100)

 

      Net cash used in investing activities

 

(343,391)

 

(214,100)

 

Cash flows from financing activities:

 

 

 

 

 

      Net cash used in financing activities

 

-

 

-

 

Net decrease in cash and cash equivalents

 

(55,829)

 

(287,582)

 

Cash and cash equivalents at beginning of period

 

1,931,823 

 

1,772,162 

 

Cash and cash equivalents at end of period

$

1,875,994 

$

1,484,580 

 

 

 

 

 

 

Supplemental Information:

 

 

 

 

 

At March 31, 2006 the Company has $1,257 of dividends payable.

 

 

 

 

 

 

The accompanying notes are an integral part of the consolidated financial statements.

 

3

 

 

 

Notes to the Consolidated Financial Statements

1. Basis of Presentation:

The unaudited interim consolidated financial statements and related notes have been prepared pursuant to the rules and regulations of the Securities and Exchange Commission. Accordingly, certain information and footnote disclosures normally included in complete financial statements prepared in accordance with generally accepted accounting principles have been omitted pursuant to such rules and regulations. The accompanying unaudited interim consolidated financial statements and related notes should be read in conjunction with the consolidated financial statements and notes thereto included in the Arrhythmia Research Technology, Inc. and subsidiary (the “Company”) Annual Report on Form 10-KSB for the year ended December 31, 2005.

The information presented reflects, in the opinion of the management of the Company, all adjustments necessary for a fair presentation of the financial results for the interim period presented.

The preparation of financial statements in conformity with accounting principles generally accepted in the United States requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements, and the reported amounts of revenues and expenses during the reporting period. Actual results could differ from those estimates. Operating results for interim periods are not necessarily indicative of results that may be expected for the entire fiscal year.

2. Inventories:

Inventories consist of the following as of:

 

March, 31,
2006

 

December 31,
2005

 

     Raw materials

$

    678,806

$

    526,412

 

     Work-in-process 

 

    440,807

 

    413,471

 

     Finished goods 

 

    706,045

 

    792,473

 

        Total 

$

1,825,658

$

1,732,356

 

3. Share-Based Compensation:

Effective January 1, 2006, the Company adopted the provisions of Statement of Financial Accounting Standards (SFAS) 123R, Share-Based Payment, which establishes accounting for equity instruments exchanged for employee services. Under the provisions of SFAS 123(R), share-based compensation cost is measured at the grant date, based on the fair value of the award, and is recognized as an expense over the employee’s requisite service period (generally the vesting period of the equity grant). Prior to January 1, 2006, the Company accounted for share-based compensation to employees in accordance with Accounting Principles Board (APB) Opinion No. 25, Accounting for stock issued to Employees, and related interpretations. The Company also followed the disclosure requirements of SFAS 123, Accounting for Stock-Based Compensation. The Company elected to adopt the modified prospective transition method as provided by SFAS 123(R) and, accordingly, financial statement amounts for the prior periods presented in the Form 10-QSB have not been restated to reflect the fair value method of expensing share-based compensation.

The Company estimates the fair value of stock options using the Black-Scholes valuation model. Key input assumptions used to estimate the fair value of stock options include the exercise price of the award, the expected option term, the expected volatility of the Company’s stock over the option’s expected term, the risk-free interest rate over the option’s expected term, and the Company’s expected annual dividend yield. The Company believes that the valuation technique and the approach utilized to develop the underlying assumptions are appropriate in calculating the fair values of the Company’s stock options. Estimates of fair value are not intended to predict actual future events or the value ultimately realized by persons who receive equity awards.

The Company recognized share-based compensation expense of $3,759 in general and administrative expense for the quarter ended March 31, 2006. No options were granted during the quarter ended March 31, 2006.

 

4

 

 

 The Company did not recognize compensation expense for employee stock option grants for the three months ended March 31, 2005, since the Company had previously adopted the provisions of SFAS 123, through disclosure only. The following illustrates the effects on net income and earnings per share for the three months ended March 31, 2005 as if the Company had applied the fair value recognition provisions of SFAS 123 to share-based employee awards.

Three months ended March 31, 2005

Net income as reported

$ 428,704

Deduct: Total share-based compensation expense determined
     under the fair value method (net of related tax effects)

(4,726)

Pro forma net income

$ 423,978

 

 

Basic and diluted earnings per share:

 

     as reported

$ 0.16

     pro forma

$ 0.16

 

 

Share-based Incentive Plan

 

At March 31, 2006, the Company had one stock option plan that includes both incentive stock options and non-statutory stock options to be granted to certain eligible employees, non-employee directors, or consultants of the Company. The maximum number of shares currently reserved for issuance is 200,000 shares. The options granted have six-year contractual terms and either vest immediately or vest annually over a five-year term.

At December 31, 2005, there were 50,000 shares available for future grants under the above stock option plan. The weighted average exercise price of options outstanding was $7.93 at March 31, 2006.

The following table presents the average price and contractual life information about options outstanding and exercisable at March 31, 2006:

Exercise Price

Number of Outstanding Shares

Weighted Average Remaining Contractual Life (years)

Options Currently Exercisable

$ 2.00

18,000

1.00

18,000

4.85

25,000

3.30

10,000

9.86

95,000

5.75

95,000

 The aggregated intrinsic value of options outstanding and vested at March 31, 2006 was $292,250 and $214,950 respectively.

 The following table summarizes the status of Company’s non-vested options since December 31, 2005:

 

Non-Vested Options

 

Number of Shares

Weighted Average Fair Value

Non-vested at December 31, 2005

21,000

$ 0.84

Granted

-

-

Vested (with intrinsic value of $48,800)

(6,000)

(1.31)

Forfeited

-

-

Non-vested at March 31, 2006

15,000

$ 0.66

 

At March 31, 2006, there was $7,662 of total unrecognized cost related to non-vested share-based compensation arrangements granted under the Plan. This cost is expected to be recognized over a weighted average period of 2.3 years.

 

5

 

 

 

4. Recent Accounting Pronouncements:

In November 2004, the FASB issued SFAS No. 151, Inventory Costs, An Amendment of ARB No. 43, Chapter 4. SFAS No. 151 clarifies that abnormal amounts of idle facility expense, freight, handling costs and wasted materials should be recognized as current period charges in all circumstances. We were required to adopt SFAS No. 151 on January 1, 2006. The adoption of SFAS No. 151 did not have a material impact on the financial statements.

In May 2005, the Financial Accounting Standards Board (“FASB”) issued SFAS No. 154, Accounting Changes and Error Corrections (“SFAS 154”), which replaces APB Opinion No. 20, Accounting Changes and SFAS No. 3, Reporting Accounting Changes in Interim Financial Statements — An Amendment of APB Opinion No. 28. SFAS 154 provides guidance on the accounting for and reporting of accounting changes and error corrections. It establishes retrospective application to prior periods’ financial statements, as the required method for reporting a change in accounting principle and the reporting of a correction of an error unless it is not practical to do so. SFAS 154 was adopted in the first quarter of fiscal 2006, and did not have a material impact.

Item 2. Management's Discussion and Analysis of Financial Condition and Results of Operations

Forward-Looking Statements

Any forward looking statements made herein are based on current expectations of the Company, involve a number of risks and uncertainties and should not be considered as guarantees of future performance. The factors that could cause actual results to differ materially include: interruptions or cancellation of existing contracts, inability to integrate acquisitions, impact of competitive products and pricing, product demand and market acceptance risks, the presence of competitors with greater financial resources than the Company, product development and commercialization risks, and changing economic conditions in developing countries. More information about factors that potentially could affect the Company's financial results is included in the Company's filings with the Securities and Exchange Commission, including its Annual Report on Form 10-KSB for the year ended December 31, 2005.

Overview

Arrhythmia Research Technology, Inc. (“ART”) is engaged in the licensing of medical software, which acquires data and analyzes electrical impulses of the heart to aid in the detection of patients who may be at risk for potentially lethal arrhythmias. Micron Products, Inc. (“Micron”), a wholly owned subsidiary, is the primary source of consolidated revenues. Micron manufactures disposable electrode sensors used as a component part in the manufacture of integrated disposable electro-physiological sensors. These disposable medical devices are used world wide in the monitoring of electric signals in various medical applications. The Company has previously acquired and integrated into Micron’s facility a custom plastic injection molding company now called the New England Molders division (“NEM”). In January 2006, the Company created a new division called Micron Integrated Technologies (“MIT”) which provides end-to-end product life cycle management through a comprehensive portfolio of value-added services such as design, engineering, prototyping, manufacturing, machining, assembly and packaging.

Results of Operations

Revenue for the three months ended March 31, 2006 was $4,269,047 versus $3,107,699 for the three months ended March 31, 2005, an increase of 37%. Micron’s medical sensors and snaps with silver surcharge contributed $375,000 to the increase in revenue. High volume precision molded products and other miscellaneous sales contributed $28,000 of the $1,161,348 total increase in revenue. NEM’s custom molded products contributed $199,000 of the increase in revenue for the first three months of 2006. MIT’s products contributed $526,000 in the first three months of 2006. MIT’s revenue resulted from orders in the defense industry. These revenues have been generated on a purchase order to purchase order basis, however we are seeking long term supply contracts that may be in place by year end. The remaining $33,350 increase in revenue came from the assembly machine business, and other ancillary unrelated manufacturing projects. There were no sales of the Company’s SAECG products in the first quarter of 2006. Non-recurring engineering and tooling revenue accounted for over $75,000 of the revenues in the three months ended March 31, 2006. Tooling and engineering revenues typically occur at the beginning of a product life cycle or when a customer changes its manufacturing source. After the design and manufacture of the prototype and/or production tooling, the Company should benefit from product sales as it begins to operate the customer owned tooling.

 

6

 

 

 

Revenue from domestic and foreign sales for the first three months is as follows:

 

 

Three Months Ending March 31,

 

 

 

2006

 

%

 

2005

 

%

 

 

United States 

$

1,703,013

 

40

$

932,907

 

30

 

Canada 

 

1,366,306

 

32

 

1,198,134

 

39

 

Europe 

 

1,064,481

 

25

 

844,875

 

27

 

Pacific Rim 

 

57,585

 

1

 

93,103

 

3

 

Other 

 

77,662

 

2

 

38,680

 

1

 

   Total 

$

4,269,047

 

100

$

3,107,699

 

100

 

The significant increase in domestic sales was a result of the MIT division’s sales and increases in the NEM division’s domestic sales. Canadian and European sales increases are the result of continued market share gains with Micron’s electrophysiological sensor and snap product line and increases in silver surcharge collected.

Cost of sales was 68% of revenue for the three months ended March 31, 2006 compared to 63% of revenue for the same period in 2005. The increase in material cost had an impact in the first quarter. Material cost in the NEM and MIT divisions are a higher percentage of revenue than Micron. Although management has been successful in stabilizing a portion of the electricity costs by negotiating a long-term purchase agreement, natural gas and resin costs continue to rise. The inability to increase our prices in the competitive global marketplace hinders passing material cost increases to our customers excluding the escalating cost of silver. The Company sells the production and prototype molding tools that it designs and qualifies for production of plastic components. These tools have a significantly lower margin than the product the tool produces. Management continues to investigate strategies to stabilize the overall gross margin without sacrificing product quality.

Selling and marketing expense was $142,455 for the three months ended March 31, 2006 as compared to $160,858 for the same period in 2005. The selling and marketing expense was 3% of sales in the three months ended March 31, 2006 as compared to 5% of sales for the same period in 2005. The Company expects selling expense as a percentage of sales to remain relatively constant over the remainder of 2006 as the Company continues to see positive results from the business development efforts.

General and administrative expense was $385,976 for the three months ended March 31, 2006 as compared to $331,755 for the same period in 2005. The increase of $54,221 in the three months ended March 31, 2006 includes the additional audit fees associated with the former auditor’s review and transition costs, and an increase in other miscellaneous corporate expenses. The cost associated with the internal control documentation necessary to comply with Section 404 of the Sarbanes Oxley Act due to an extension of the implementation date will begin in the fourth quarter of 2006.

Research and development expense was $17,456 for the three months ended March 31, 2006 as compared to $16,961 for the same period in 2005. The expense was related to ART’s product, Predictor®7. Although base development work on Predictor 7 has been completed, product testing costs were expended to support a research project utilizing ART’s proprietary Signal Averaged ECG products and patented algorithms.

Other expense, net was $14,887 versus income of $6,497 for the three months ended March 31, 2006 and 2005, respectively. The doubling of interest income from the Company’s cash balance in the first three months of 2006 as compared to 2005 partially offset the loss associated with the retirement of a direct financed customer tool. A portion of this loss included the replacement of older factory equipment with new more efficient equipment.

Income taxes as a percent of income before income taxes were 35% for the three months ended March 31, 2006 and 2005. Management will continue to seek to implement any tax planning opportunities that could effectively reduce the Company’s income tax provision in the future.

Liquidity and Capital Resources

 

Working capital was $5,831,681 on March 31, 2006 compared to $5,386,899 at December 31, 2005, an increase of $444,782. The higher accounts receivable reflects the increase in revenues. This increase was partially offset by an increase in accounts payable. Capital investment could decrease working capital further with any significant investment resulting from any future acquisition of assets or businesses, significant expansion of production capacity, a medical study, or further software development.

 

 

7

 

 

 

Net capital expenditures were $343,391 for the first three months of 2006 as compared to $214,100 for the same period in 2005. The majority of the capital expenditures in the first three months of 2006 were for the acquisition of additional production machinery and equipment, including upgrades in and replacement of existing machinery and tooling.

The Company has an unsecured $1,000,000 credit line with a large multinational bank. No funds have been drawn down on the line as of March 31, 2006 or December 31, 2005.

The Company expects to meet cash demands for its operations at current levels with current operating cash flows for the foreseeable future.

Critical Accounting Policies

The preparation of financial statements and related disclosures in conformity with generally accepted accounting principles requires management to make judgments, assumptions and estimates that affect the amounts reported. Certain of these significant accounting policies are considered to be critical accounting policies, as defined below.

A critical accounting policy is defined as one that is both material to the presentation of the Company’s financial statements and requires management to make difficult, subjective, and complex judgments that could have a material effect on the Company’s financial condition and results of operations. Specifically, critical accounting estimates have the following attributes: 1) the Company is required to make assumptions about matters that are highly uncertain at the time of the estimate; and 2) different estimates the Company could reasonably have used, or changes in the estimate that are reasonably likely to occur, would have a material effect on the Company’s financial condition or results of operations.

Estimates and assumptions about future events and their effects cannot be determined with certainty. The Company bases its estimates on historical experience and on various other assumptions believed to be applicable and reasonable under the circumstances. These estimates may change as new events occur, as additional information is obtained and as the Company’s operating environment changes. These changes have historically been minor and have been included in the consolidated financial statements as soon as they became known. In addition, management is periodically faced with uncertainties, the outcomes of which are not within its control and will not be known for prolonged periods of time. These uncertainties are discussed in the section above entitled “Forward-looking Statements.” Based on a critical assessment of its accounting policies and the underlying judgments and uncertainties affecting the application of those policies, management believes that the Company’s consolidated financial statements are fairly stated in accordance with generally accepted accounting principles, and present a meaningful presentation of the Company’s financial condition and results of operations.

Management believes that the following are critical accounting policies:

Revenue Recognition and Accounts Receivable

Revenues from the sale of products are recorded when the product is shipped, title and risk of loss have transferred to the purchaser, payment terms are fixed or determinable and payment is reasonably assured.

The financing of customer purchased tooling utilizes the direct financing method of revenue recognition. This requires the gain or loss on the sale of the tooling to be recorded at the time the tool is put into service while the expected payments are reflected as a lease receivable.

Based on management’s on-going analysis of accounts receivable balances, and after the initial recognition of the revenue, if an event occurs which may adversely affect the ultimate collectibility of the related receivable, management will record an allowance for the bad debt. Bad debts have not had a significant impact on the Company’s financial condition, results of operations or cash flows.

Inventory and Inventory Reserves

The Company values its inventory at the lower of cost or market. The Company reviews its inventory for quantities in excess of production requirements, obsolescence and for compliance with internal quality specifications. Any adjustments to inventory would be equal to the difference between the cost of inventory and the estimated net market value based upon assumptions about future demand, market conditions and expected cost to distribute those products to market. If actual market conditions are less favorable than those projected by management, additional inventory reserves may be required.

 

8

 

 

 

 The Company maintains a reserve for excess, slow moving, and obsolete inventory as well as inventory with a carrying value in excess of its net realizable value. A review of inventory on hand is made at least annually and a provision for excess, slow moving, and obsolete inventory is recorded. The review is based on several factors including a current assessment of future product demand, historical experience, and product expiration.

Deferred Tax Assets

The Company assesses its deferred tax assets based upon a more likely than not to be realized criteria. The Company considers future taxable income and ongoing prudent and feasible tax planning strategies in assessing the need for the valuation allowance.

Asset Impairment – Goodwill

The Company reviews the valuation of goodwill and intangible assets to assess potential impairments on an annual basis. The management evaluates the carrying value of goodwill and other intangible assets in accordance with the guidelines set forth in SFAS 142. The value assigned to intangible assets is determined by a valuation based on estimates and judgment regarding expectations for the success and life cycle of products acquired. To test for impairment, present values of an estimate of future discounted cash flows related to the intangible assets are calculated compared to the value of the intangible asset. Impairment may have a material adverse effect on the Company’s financial condition or results of operations. There was no impairment as of March 31, 2006.

Asset Impairment – Long Lived Assets

The Company assesses the impairment of long-lived assets whenever events or changes in circumstances indicate that the carrying value may not be fully recoverable. When it is determined that the carrying value of such assets may not be recoverable, the Company generally measures any impairment based on projected undiscounted future cash flows attributed to the asset and its carrying value. If the carrying value exceeds the future discounted cash flows, asset impairment would be recorded.

Item 3. Controls and Procedures

As of the end of the period covered by this Quarterly Report, the Company’s management, with the participation of the Company’s Chief Executive Officer and Chief Financial Officer (“the Certifying Officers”), conducted evaluations of the Company’s disclosure controls and procedures. As defined under Sections 13a – 15(e) and 15d – 15(e) of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), the term “disclosure controls and procedures” means controls and other procedures of an issuer that are designed to ensure that information required to be disclosed by the issuer in the reports that it files or submits under the Exchange Act is recorded, processed, summarized and reported, within the time periods specified in the Commission’s rules and forms. Disclosure controls and procedures include without limitation, controls and procedures designed to ensure that information required to be disclosed by an issuer in the reports that it files or submits under the Exchange Act is accumulated and communicated to the issuer’s management, included the Certifying Officers, to allow timely decisions regarding required disclosures. Based on this evaluation, the Certifying Officers have concluded that the Company’s disclosure controls and procedures were effective to ensure that material information is recorded, processed, summarized and reported by management of the Company on a timely basis in order to comply with the Company’s disclosure obligations under the Exchange Act and the rules and regulations promulgated thereunder.

Further, there were no changes in the Company’s internal control over financial reporting during the Company’s first fiscal quarter that materially affected, or are reasonably likely to materially affect, the Company’s internal control over financial reporting.

 

9

 

 

 

PART II - OTHER INFORMATION

Item 6. Exhibits

 

(a)

Exhibits

  3.0     Articles of Incorporation(a)

  3.1     By-laws(b)

10.40* Employment agreement between James E. Rouse and the Company dated October 5th, 2001(c)

10.41   Asset Purchase Agreement, dated May 7, 2004, between Micron Products, Inc. and Shrewsbury Molders, Inc.(d)

31.1     Certification of the CEO pursuant to Rule 13a-14(a) or Rule 15(d)-14(a) on page X-1.

31.2     Certification of the CFO pursuant to Rule 13a-14(a) or Rule 15(d)-14(a) on page X-2.

32.1     Certification pursuant to 18 U.S.C. §1350 as adopted pursuant to Section 906 of the

                   Sarbanes-Oxley Act of 2002 on page X-3.

32.2     Certification pursuant to 18 U.S.C. §1350 as adopted pursuant to Section 906 of the

                   Sarbanes-Oxley Act of 2002 on page X-4.

* Indicates a management contract or compensatory plan required to be filed as an exhibit.

 

(a)

Incorporated by reference from the Company’s Registration Statement on Form S-18 as filed with the Commission in April 1988, Registration Statement No. 33-20945-FW.

 

(b)

Incorporated by reference from the Company’s Form 10-Q for period ended September 30, 2002 as filed with the Commission in November 2002.

 

(c)

Incorporated by reference from the Company’s Form 10-Q as exhibit 10.10 for period ended September 30, 2002 as filed with the Commission in November 2002.

 

(d)

Incorporated by reference from the Company’s Form 8-K as filed with the Commission on May 21, 2004.

 

SIGNATURES

In accordance with the requirements of the Securities Exchange Act of 1934, the registrant caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

 

ARRHYTHMIA RESEARCH TECHNOLOGY, INC.

 

By:

/s/ James E. Rouse        

 

 

James E. Rouse

 

 

President and Chief Executive Officer

 

 

(Principal Executive Officer)

 

 

 

 

By: 

/s/ David A. Garrison        

 

 

David A. Garrison

 

 

Executive Vice President and Chief Financial Officer

 

 

(Principal Financial and Accounting Officer)

May 12, 2006

 

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