FDA Inspection 873262 — Cadila Pharmaceuticals Limited

Cadila Pharmaceuticals Limited — FEI 3002806711

The FDA completed an inspection of Cadila Pharmaceuticals Limited on March 28, 2014 in Ankleshwar. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
March 28, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ankleshwar (India)