FDA Inspection 694644 — Aurobindo Pharma Limited

Aurobindo Pharma Limited — FEI 3007373532

The FDA completed an inspection of Aurobindo Pharma Limited on Jul 30, 2010 in Jedcherla Mandal, Mahabubnagar. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 30, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jedcherla Mandal, Mahabubnagar (India)

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