FDA Inspection 1094880 — Cipla Limited

Cipla Limited — FEI 3008581988

The FDA completed an inspection of Cipla Limited on May 17, 2019 in Pithampur, District Dhar. 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
May 17, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pithampur, District Dhar (India)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.