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FDA Inspection 694644 — Aurobindo Pharma Limited

Aurobindo Pharma Limited — FEI 3007373532

The FDA completed an inspection of Aurobindo Pharma Limited on July 30, 2010 in Jedcherla Mandal, Mahabubnagar. 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
July 30, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jedcherla Mandal, Mahabubnagar (India)

Facility

Other inspections at this facility

  • 1169446 (VAI Tue May 10 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1105823 (OAI Fri Sep 27 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1022788 (NAI Sat Jun 24 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 927596 (NAI Fri Mar 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 787128 (NAI Tue Jun 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources