FDA Inspection 636493 — Aurobindo Pharma Limited

Aurobindo Pharma Limited — FEI 3007373532

The FDA completed an inspection of Aurobindo Pharma Limited on Oct 13, 2009 in Jedcherla Mandal, Mahabubnagar. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 13, 2009
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.