FDA Inspection 1286862 — Aurobindo Pharma Limited

Aurobindo Pharma Limited — FEI 3004446312

The FDA completed an inspection of Aurobindo Pharma Limited on September 5, 2025 in Medchal. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

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