FDA inspection
Intercos Europe SpA: FDA inspection ending Sep 11, 2019
FDA inspection 1110083 · No Action Indicated (NAI) · Dovera
Key facts
| Inspection ID | 1110083 |
|---|---|
| Firm | Intercos Europe SpA |
| FEI number | 3005291719 |
| Address | Km. 21 150, Strada Provinciale Di Orzinuovi 472 |
| City | Dovera |
| Country | Italy |
| Fiscal year | 2019 |
| Inspection end date | Sep 11, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data