FDA Warning Letter — Glenmark Pharmaceuticals Inc USA

Case 637162 — FEI 3011585599

The FDA took a Warning Letter action against Glenmark Pharmaceuticals Inc USA on June 20, 2023 (Monroe, NC). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Glenmark Pharmaceuticals Inc USA
Date
June 20, 2023
Fiscal Year
2023
Product Type
Drugs
Center
CDER
Location
Monroe, NC (United States)