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FDA Inspection 1078911 — Cipla Limited

Cipla Limited — FEI 3004081307

The FDA completed an inspection of Cipla Limited on January 28, 2019 in Salcette. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 28, 2019
Fiscal Year
2019
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Salcette (India)

Facility

Other inspections at this facility

  • 1240813 (VAI Fri Jun 21 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1178952 (OAI Fri Aug 26 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1103305 (OAI Fri Sep 27 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1069950 (VAI Fri Sep 28 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1015874 (VAI Fri Jun 16 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources