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FDA Warning Letter — Virginia Center for Reproductive Medicine

Case 583610 — FEI 3003939253

The FDA took a Warning Letter action against Virginia Center for Reproductive Medicine on July 1, 2019 (Reston, VA). The action was issued by CBER and concerns biologics products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Virginia Center for Reproductive Medicine
Date
July 1, 2019
Fiscal Year
2019
Product Type
Biologics
Center
CBER
Location
Reston, VA (United States)

Facility

Recent inspections

  • 1280934 (NAI Thu Aug 28 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1218271 (VAI Wed Sep 20 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1156160 (VAI Fri Oct 29 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1081380 (OAI Mon Feb 25 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 833772 (OAI Wed Jun 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Other compliance actions

FDA data resources