FDA Inspection 768491 — Cipla Ltd.

Cipla Ltd. — FEI 3005857289

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

Inspection Details

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

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