FDA Inspection 780312 — 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 Apr 5, 2012 in Termoli. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Apr 5, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Termoli (Italy)

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