FDA Warning Letter — Virginia Center for Reproductive Medicine

Case 409387 — FEI 3003939253

The FDA took a Warning Letter action against Virginia Center for Reproductive Medicine on September 10, 2013 (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
September 10, 2013
Fiscal Year
2013
Product Type
Biologics
Center
CBER
Location
Reston, VA (United States)