FDA Inspection 837223 — Cipla Limited

Cipla Limited — FEI 3004081307

The FDA completed an inspection of Cipla Limited on May 30, 2013 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
May 30, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Salcette (India)