FDA Inspection 1332838 — 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 Jul 25, 2025 in Novi Ligure. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 25, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Novi Ligure (Italy)

Additional Details

Mutual Recognition Agreement (MRA)

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