FDA Inspection 1045859 — Syngene International Limited

Syngene International Limited — FEI 3007907068

The FDA completed an inspection of Syngene International Limited on January 26, 2018 in Bengalore. 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
January 26, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Bengalore (India)

Additional Details

Bioanalytical BA/BE