FDA Inspection 929021 — Megafine Pharma (P) Limited

Megafine Pharma (P) Limited — FEI 3005694111

The FDA completed an inspection of Megafine Pharma (P) Limited on May 15, 2015 in Nashik. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 15, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nashik (India)