FDA Warning Letter — Lupin Limited

Case 532465 — FEI 3004819820

The FDA took a Warning Letter action against Lupin Limited on November 6, 2017 (Verna, 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
November 6, 2017
Fiscal Year
2018
Product Type
Drugs
Center
CDER
Location
Verna (India)