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66 -- Radiation Monitor

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Reference-Number-A71456Federal

Contract Overview

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The Food and Drug Administration plans to award a sole source purchase order to Radcal Corporation of Monrovia, California, for the provision of specific radiation monitoring equipment. The order includes six Radcal FBH Radiation Monitors with converters and 4-meter cables (Model 1015), five additional units of Model 1015FBH, six ion chambers (Models 10X5-6L and 10X5-180), and five mammography ion chambers (Model 10-5-6m). The FDA currently uses a large inventory of the Model 1015 FB x-ray monitors, which were custom-designed for their use; therefore, introducing different equipment would require significant procedural changes, system modifications, and retraining of inspectors. This procurement is being conducted as a simplified acquisition under FAR 12.6 and is not open to competitive bids, although other sources may submit descriptive literature to demonstrate their capability. The sole source approach is justified by the need for compatibility with existing equipment and procedures essential to FDA inspection activities. The contract was posted on July 18, 2003, under the reference number A71456.

General Info

FDA awards sole source contract to Radcal for compatible radiation monitoring equipment procurement.

Agency

N/A

NAICS

334519 - Other Measuring and Controlling Device Manufacturing

Place of Performance

Not specified

Set-Aside

NONE

Documents

0

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Timeline

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Organization & Contact Information

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AgencyN/A
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Full Description

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The Food and Drug Administration intends to award a Purchase order on a sole source basis to Radcal Corporation, of Monrovia, California. Radcal shall provide FDA six (6) Radcal FBH Radiation Monitor with converter, 4-m cable and options FB, Model number 1015 and five (5) Model number 1015FBH; six (6) Ion chamber, Model number 10X5-6L and 10X5-180; five (5) Mammography ion chamber, Model number 10-5-6m. The FDA currently owns a significant amount of the 1015 FB x-ray monitor which has been designed especially for FDA. The equipment has been incorporated in inspection procedures and any differences in the equipment would involve substantial changes in procedures, modification and retraining of inspectors. This is not a request for quotes; however, sources may submit descriptive literature, which fully demonstrate their capability, which will be considered by the agency. This sole source procurement is being awarded as a simplified acquisition in accordance with FAR 12.6.

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