FDA inspection
NUVOAIR AB: FDA inspection ending Sep 22, 2022
FDA inspection 1180862 · Voluntary Action Indicated (VAI) · Stockholm
Key facts
| Inspection ID | 1180862 |
|---|---|
| Firm | NUVOAIR AB |
| FEI number | 3013744763 |
| Address | Riddargatan 17d 3rd Fl |
| City | Stockholm |
| Country | Sweden |
| Fiscal year | 2022 |
| Inspection end date | Sep 22, 2022 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None 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