FDA Inspection 1195646 — Megafine Pharma (P) Limited

Megafine Pharma (P) Limited — FEI 3005694111

The FDA completed an inspection of Megafine Pharma (P) Limited on Jan 24, 2023 in Nashik. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 24, 2023
Fiscal Year
2023
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.