FDA inspection
Bios S.r.l.: FDA inspection ending Jul 13, 2017
FDA inspection 1020085 · Voluntary Action Indicated (VAI) · Vimodrone
Key facts
| Inspection ID | 1020085 |
|---|---|
| Firm | Bios S.r.l. |
| FEI number | 3008108972 |
| Address | Via Guido Rossa 10/12 |
| City | Vimodrone |
| Country | Italy |
| Fiscal year | 2017 |
| Inspection end date | Jul 13, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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
- 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