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FDA Inspection 850780 — Zydus Lifesciences Limited

Zydus Lifesciences Limited — FEI 3002984011

The FDA completed an inspection of Zydus Lifesciences Limited on August 19, 2013 in Taluka Sanand, Ahmedabad. 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
August 19, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Taluka Sanand, Ahmedabad (India)

Facility

Other inspections at this facility

  • 1177670 (VAI Fri Aug 05 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1088772 (OAI Fri May 03 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1090231 (NAI Fri Mar 22 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1047493 (NAI Fri Feb 09 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1006533 (NAI Thu Feb 16 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources