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This Government Contract opportunity from Department Of Defense was posted on May 28, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

FDA Regulatory Compliance and Product Specialist Coordination

Closed
Federal

Contract Overview

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This contract requires the provision of technical data and coordination with Defense Logistics Agency (DLA) product specialists to confirm FDA regulatory status for a Class I medical device. The work involves ensuring compliance with FDA regulations by collaborating with experts to verify the classification of the device, which is essential for meeting medical supply chain requirements. The contract is designated as a subcontract under the NAICS code 541611, which pertains to administrative management and general management consulting services. The contracting agency is the Department of Defense through the Medical Supply Chain MD SURG FSF office, with performance taking place at APO 09461-9997. The solicitation was posted on May 28, 2026, and responses are due by June 3, 2026, indicating a relatively short timeframe for submission. This effort supports the regulatory and logistical aspects of medical device compliance in the defense sector, ensuring that products meet established federal guidelines before distribution or use.

General Info

Provide technical data and confirm FDA status for Class I medical device under DoD subcontract.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

NAICS

541611 - Administrative Management and General Management Consulting Services View NAICS

Place of Performance

APO, AE, 09461-9997, US

Set-Aside

NONE

Documents

(0)

No documents available

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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
Office AddressN/A
ContactsNo contact information available

Full Description

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Provide technical data and coordinate with DLA product specialists for FDA regulatory confirmation of Class I medical device status.