FDA inspection
Fidia Farmaceutici S.p.A.: FDA inspection ending Nov 10, 2016
FDA inspection 998561 · Voluntary Action Indicated (VAI) · Abano Terme
Key facts
| Inspection ID | 998561 |
|---|---|
| Firm | Fidia Farmaceutici S.p.A. |
| FEI number | 3002806986 |
| Address | Via Ponte Della Fabbrica 3/A |
| City | Abano Terme |
| Country | Italy |
| Fiscal year | 2017 |
| Inspection end date | Nov 10, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Project Evaluation: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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