FDA Inspection 943821 — Cipla Limited

Cipla Limited — FEI 3004081307

The FDA completed an inspection of Cipla Limited on April 17, 2015 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 17, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Salcette (India)