FDA Inspection 730085 — Megafine Pharma (P) Limited

Megafine Pharma (P) Limited — FEI 3005694111

The FDA completed an inspection of Megafine Pharma (P) Limited on Jun 2, 2011 in Nashik. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 2, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nashik (India)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.