FDA Inspection 891868 — Cipla Limited

Cipla Limited — FEI 3002806691

The FDA completed an inspection of Cipla Limited on July 25, 2014 in Bengaluru. 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
July 25, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bengaluru (India)