FDA Inspection 1342744 — FIS - Fabbrica Italiana Sintetici S.P.A.

FIS - Fabbrica Italiana Sintetici S.P.A. — FEI 3002806961

The FDA completed an inspection of FIS - Fabbrica Italiana Sintetici S.P.A. on Mar 6, 2026 in Montecchio Maggiore. 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
Mar 6, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Montecchio Maggiore (Italy)

Additional details

Mutual Recognition Agreement (MRA)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.