FDA Warning Letter — GCP Laboratories

Case 57183 — FEI 1019058

The FDA took a Warning Letter action against GCP Laboratories on August 21, 2009 (Gulfport, MS). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
GCP Laboratories
Date
August 21, 2009
Fiscal Year
2009
Product Type
Drugs
Center
CDER
Location
Gulfport, MS (United States)