FDA Inspection 1110083 — Intercos Europe SpA

Intercos Europe SpA — FEI 3005291719

The FDA completed an inspection of Intercos Europe SpA on September 11, 2019 in Dovera. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 11, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dovera (Italy)