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FDA Inspection 988000 — Megafine Pharma (P) Limited

Megafine Pharma (P) Limited — FEI 3006688078

The FDA completed an inspection of Megafine Pharma (P) Limited on September 23, 2016 in Vapi. 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
September 23, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vapi (India)

Facility

Other inspections at this facility

  • 1207908 (VAI Fri May 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1121027 (OAI Fri Feb 21 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1058583 (OAI Fri Jun 15 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 828506 (VAI Wed Mar 13 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources