FDA Inspection 684552 — Aurobindo Pharma Ltd

Aurobindo Pharma Ltd — FEI 3004021229

The FDA completed an inspection of Aurobindo Pharma Ltd on September 24, 2010 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 24, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Medchal (India)