FDA Inspection 659697 — BASF SE

BASF SE — FEI 3002903906

The FDA completed an inspection of BASF SE on March 17, 2010 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
March 17, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ludwigshafen Am Rhein (Germany)