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FDA Inspection 643147 — Glenmark Pharmaceuticals Limited

Glenmark Pharmaceuticals Limited — FEI 3005757050

The FDA completed an inspection of Glenmark Pharmaceuticals Limited on November 13, 2009 in Solan. 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
November 13, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Solan (India)

Facility

Other inspections at this facility

  • 1172425 (OAI Wed Jun 22 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1070594 (NAI Fri Sep 21 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1031652 (VAI Sat Nov 11 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 929619 (VAI Fri May 29 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 802324 (NAI Fri Aug 24 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources