FDA Warning Letter — Megafine Pharma (P) Limited

Case 479195 — FEI 3005694111

The FDA took a Warning Letter action against Megafine Pharma (P) Limited on May 19, 2016 (Nashik, 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
Megafine Pharma (P) Limited
Date
May 19, 2016
Fiscal Year
2016
Product Type
Drugs
Center
CDER
Location
Nashik (India)