FDA Inspection 1077094 — Jubilant Pharmova Limited

Jubilant Pharmova Limited — FEI 3003144728

The FDA completed an inspection of Jubilant Pharmova Limited on December 18, 2018 in Mysore. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
December 18, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mysore (India)