FDA Inspection 940768 — Aurobindo Pharma Ltd

Aurobindo Pharma Ltd — FEI 3004021229

The FDA completed an inspection of Aurobindo Pharma Ltd on June 26, 2015 in Medchal. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 26, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Medchal (India)