FDA Warning Letter — Glenmark Pharmaceuticals Limited

Case 582701 — FEI 3005757050

The FDA took a Warning Letter action against Glenmark Pharmaceuticals Limited on October 3, 2019 (Solan, India). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Glenmark Pharmaceuticals Limited
Date
October 3, 2019
Fiscal Year
2020
Product Type
Drugs
Center
CDER
Location
Solan (India)