FDA Warning Letter — Pfizer, Inc.

Case 92384 — FEI 1211022

The FDA took a Warning Letter action against Pfizer, Inc. on April 9, 2010 (Groton, CT). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Pfizer, Inc.
Date
April 9, 2010
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Groton, CT (United States)