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FDA Inspection 962120 — Lupin Limited

Lupin Limited — FEI 3002807511

The FDA completed an inspection of Lupin Limited on February 19, 2016 in Mandideep. 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
February 19, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mandideep (India)

Facility

Other inspections at this facility

  • 1191374 (OAI Wed Nov 23 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1073522 (OAI Tue Dec 04 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 748307 (VAI Fri Sep 23 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 632615 (VAI Mon Nov 30 2009 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 552469 (OAI Wed Nov 12 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources