FDA Inspection 1142089 — AnaBioTec nv

AnaBioTec nv — FEI 3003990527

The FDA completed an inspection of AnaBioTec nv on September 15, 2020 in Evergem. 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
September 15, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Evergem (Belgium)

Additional Details

Mutual Recognition Agreement (MRA)