FDA Inspection 1015874 — Cipla Limited

Cipla Limited — FEI 3004081307

The FDA completed an inspection of Cipla Limited on June 16, 2017 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
June 16, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Salcette (India)