FDA Inspection 1120482 — Cadila Pharmaceuticals Limited

Cadila Pharmaceuticals Limited — FEI 3007684569

The FDA completed an inspection of Cadila Pharmaceuticals Limited on Feb 14, 2020 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
Feb 14, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ahmedabad (India)

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