FDA Inspection 959713 — BASF AS avd Sandefjord

BASF AS avd Sandefjord — FEI 3000212124

The FDA completed an inspection of BASF AS avd Sandefjord on December 11, 2015 in Sandefjord. 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 11, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sandefjord (Norway)