FDA Warning Letter — Wockhardt, Ltd.

Case 495920 — FEI 3002808500

The FDA took a Warning Letter action against Wockhardt, Ltd. on December 23, 2016 (Ankleshwar, India). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Wockhardt, Ltd.
Date
December 23, 2016
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Ankleshwar (India)