FDA Inspection 1217681 — Bioindustria Laboratorio Italiano Medicinali S.p.A

Bioindustria Laboratorio Italiano Medicinali S.p.A — FEI 3002717526

The FDA completed an inspection of Bioindustria Laboratorio Italiano Medicinali S.p.A on February 24, 2023 in Novi Ligure. 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
February 24, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Novi Ligure (Italy)

Additional Details

Mutual Recognition Agreement (MRA)