FDA Warning Letter — Hikma Pharmaceuticals USA INC.

Case 53122 — FEI 1510690

The FDA took a Warning Letter action against Hikma Pharmaceuticals USA INC. on March 30, 2009 (Columbus, OH). 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
March 30, 2009
Fiscal Year
2009
Product Type
Drugs
Center
CDER
Location
Columbus, OH (United States)