FDA Inspection 1276304 — FIS - Fabbrica Italiana Sintetici SpA

FIS - Fabbrica Italiana Sintetici SpA — FEI 3002808541

The FDA completed an inspection of FIS - Fabbrica Italiana Sintetici SpA on Oct 28, 2022 in Lonigo. 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
Oct 28, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lonigo (Italy)

Additional details

Mutual Recognition Agreement (MRA)

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