FDA Inspection 768491 — Cipla Ltd.

Cipla Ltd. — FEI 3005857289

The FDA completed an inspection of Cipla Ltd. on November 17, 2011 in Bangalore. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 17, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bangalore (India)