FDA Warning Letter — Megafine Pharma (P) Limited

Case 510862 — FEI 3006688078

The FDA took a Warning Letter action against Megafine Pharma (P) Limited on February 24, 2017 (Vapi, 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
February 24, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Vapi (India)