FDA Warning Letter — BioReliance Corporation

Case 45718 — FEI 1122041

The FDA took a Warning Letter action against BioReliance Corporation on January 5, 2009 (Rockville, MD). The action was issued by CBER and concerns biologics products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
BioReliance Corporation
Date
January 5, 2009
Fiscal Year
2009
Product Type
Biologics
Center
CBER
Location
Rockville, MD (United States)