FDA Warning Letter — Hikma Pharmaceuticals USA, Inc.

Case 213453 — FEI 2250102

The FDA took a Warning Letter action against Hikma Pharmaceuticals USA, Inc. on February 6, 2012 (Eatontown, NJ). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Hikma Pharmaceuticals USA, Inc.
Date
February 6, 2012
Fiscal Year
2012
Product Type
Drugs
Center
CDER
Location
Eatontown, NJ (United States)