FDA Inspection 1110083 — Intercos Europe SpA

Intercos Europe SpA — FEI 3005291719

The FDA completed an inspection of Intercos Europe SpA on Sep 11, 2019 in Dovera. 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
Sep 11, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dovera (Italy)

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