FDA Inspection 1317510 — FIS - Fabbrica Italiana Sintetici S.P.A

FIS - Fabbrica Italiana Sintetici S.P.A — FEI 3008347496

The FDA completed an inspection of FIS - Fabbrica Italiana Sintetici S.P.A on Sep 22, 2023 in Termoli. 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
Sep 22, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Termoli (Italy)

Additional details

Mutual Recognition Agreement (MRA)

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