FDA Inspection 961470 — FIS - Fabbrica Italiana Sintetici SpA

FIS - Fabbrica Italiana Sintetici SpA — FEI 3002808541

The FDA completed an inspection of FIS - Fabbrica Italiana Sintetici SpA on Feb 25, 2016 in Lonigo. 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
Feb 25, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lonigo (Italy)

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