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FDA Inspection 940719 — Cipla Limited

Cipla Limited — FEI 3008581988

The FDA completed an inspection of Cipla Limited on August 7, 2015 in Pithampur, District Dhar. 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
August 7, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pithampur, District Dhar (India)

Facility

Other inspections at this facility

  • 1198343 (OAI Fri Feb 17 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1094880 (NAI Fri May 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1048005 (VAI Fri Apr 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 821114 (VAI Fri Mar 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 806838 (NAI Fri Nov 02 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources