FDA Inspection 1173461 — Cadila Pharmaceuticals Limited

Cadila Pharmaceuticals Limited — FEI 3007684569

The FDA completed an inspection of Cadila Pharmaceuticals Limited on Jun 17, 2022 in Ahmedabad. 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
Jun 17, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Ahmedabad (India)

Additional Details

Clinical BA/BE

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