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FDA Inspection 1035804 — Panacea Biotec Pharma Limited

Panacea Biotec Pharma Limited — FEI 3007187282

The FDA completed an inspection of Panacea Biotec Pharma Limited on December 13, 2017 in Solan. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 13, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Solan (India)

Facility

Other inspections at this facility

  • 1220156 (OAI Thu Oct 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1172929 (OAI Wed Jun 08 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1093361 (NAI Tue Apr 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 954394 (VAI Fri Dec 11 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 852630 (VAI Fri Oct 25 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources