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FDA Inspection 1084973 — Cipla, Ltd.

Cipla, Ltd. — FEI 3002806702

The FDA completed an inspection of Cipla, Ltd. on March 20, 2019 in Kurkumbh Village, Dist. Pune. 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
March 20, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kurkumbh Village, Dist. Pune (India)

Facility

Other inspections at this facility

  • 1236690 (VAI Wed May 08 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1073182 (NAI Fri Nov 30 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 997481 (VAI Fri Dec 09 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 882706 (NAI Fri May 23 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 755727 (VAI Thu Dec 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources