FDA Inspection 1286862 — Aurobindo Pharma Limited

Aurobindo Pharma Limited — FEI 3004446312

The FDA completed an inspection of Aurobindo Pharma Limited on Sep 5, 2025 in Medchal. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Sep 5, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Medchal (India)

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