FDA Warning Letter — Jubilant Generics Limited

Case 569799 — FEI 3006895982

The FDA took a Warning Letter action against Jubilant Generics Limited on March 6, 2019 (Bhagwanpur, 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
Jubilant Generics Limited
Date
March 6, 2019
Fiscal Year
2019
Product Type
Drugs
Center
CDER
Location
Bhagwanpur (India)