FDA Inspection 1037843 — Gulbrandsen Technologies (India) Private Limited

Gulbrandsen Technologies (India) Private Limited — FEI 3006216494

The FDA completed an inspection of Gulbrandsen Technologies (India) Private Limited on December 8, 2017 in Jhagadia. 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
December 8, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jhagadia (India)