FDA Inspection 948221 — Jubilant Pharmova Limited

Jubilant Pharmova Limited — FEI 3003144728

The FDA completed an inspection of Jubilant Pharmova Limited on October 16, 2015 in Mysore. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 16, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mysore (India)