FDA Inspection 1151063 — BENECHIM SPRL

BENECHIM SPRL — FEI 3004293182

The FDA completed an inspection of BENECHIM SPRL on January 26, 2021 in Lessines. 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
January 26, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lessines (Belgium)

Additional Details

Mutual Recognition Agreement (MRA)