FDA Inspection 1289396 — BASF SE

BASF SE — FEI 3002903906

The FDA completed an inspection of BASF SE on August 29, 2024 in Ludwigshafen Am Rhein. 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
August 29, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ludwigshafen Am Rhein (Germany)

Additional Details

Mutual Recognition Agreement (MRA)