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FDA Inspection 1231774 — Jubilant Generics Limited

Jubilant Generics Limited — FEI 3006895982

The FDA completed an inspection of Jubilant Generics Limited on February 2, 2024 in Bhagwanpur. 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 2, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bhagwanpur (India)

Facility

Other inspections at this facility

  • 1175958 (OAI Mon Aug 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1137148 (OAI Fri Mar 12 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1112459 (OAI Wed Nov 06 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1007262 (NAI Thu Mar 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 971357 (VAI Fri Apr 08 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources