FDA Inspection 711843 — Aurobindo Pharma Limited

Aurobindo Pharma Limited — FEI 3004021263

The FDA completed an inspection of Aurobindo Pharma Limited on December 22, 2010 in Sangareddy. 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
December 22, 2010
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sangareddy (India)