FDA Inspection 788228 — Jubilant Pharmova Limited

Jubilant Pharmova Limited — FEI 3003144728

The FDA completed an inspection of Jubilant Pharmova Limited on May 31, 2012 in Mysore. 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
May 31, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mysore (India)