FDA Warning Letter — Raritan Pharmaceuticals, Inc.

Case 516099 — FEI 3004083931

The FDA took a Warning Letter action against Raritan Pharmaceuticals, Inc. on June 20, 2017 (East Brunswick, 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
Raritan Pharmaceuticals, Inc.
Date
June 20, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
East Brunswick, NJ (United States)