FDA Inspection 959713 — BASF AS Avd Sandefjord

BASF AS Avd Sandefjord — FEI 3000212124

The FDA completed an inspection of BASF AS Avd Sandefjord on Dec 11, 2015 in Sandefjord. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 11, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sandefjord (Norway)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.