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This Government Contract opportunity from Department Of Defense was posted on May 20, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Medical Device Regulatory Compliance and Quality Assurance

Closed
Federal

Contract Overview

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This contract entails providing quality assurance and regulatory compliance services focused on ensuring that repair parts conform to the DLA Master List RA001, medical device standards, and inspection requirements. The work is critical to maintaining the integrity and safety of medical devices used by the Department of Defense. The contract is categorized as a subcontract and falls under the NAICS code 541380, which relates to testing laboratories. The Department of Defense's Medical Supply Chain MD SURG FSF office is responsible for the contract, with the place of performance designated as Goose Creek, zip code 29445. The solicitation was posted on May 20, 2026, and responses are due by May 26, 2026. The contract does not specify a set-aside type or organization type, and further details can be accessed through the provided government procurement link.

General Info

Provide quality assurance and compliance services for medical device repair parts at Goose Creek.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSFView Agency

NAICS

541380 - Testing Laboratories and ServicesView NAICS

Place of Performance

GOOSE CREEK, SC, 29445-0000, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DS-26-T-091Z.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

RESERVOIR, BLOOD-FLU

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Timeline

PhaseClosed
Posted

subcontract

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF
View Agency Profile
Office AddressN/A
ContactsNo contact information available

Full Description

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Quality assurance and regulatory compliance services to ensure the repair part meets DLA Master List RA001, medical device standards, and inspection requirements.

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