FDA Warning Letter — Lupin Limited

Case 572345 — FEI 3002807511

The FDA took a Warning Letter action against Lupin Limited on September 10, 2019 (Mandideep, 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
Lupin Limited
Date
September 10, 2019
Fiscal Year
2019
Product Type
Drugs
Center
CDER
Location
Mandideep (India)