FDA inspection
ScandiDos AB: FDA inspection ending Jul 12, 2018
FDA inspection 1058626 · Voluntary Action Indicated (VAI) · Uppsala
Key facts
| Inspection ID | 1058626 |
|---|---|
| Firm | ScandiDos AB |
| FEI number | 3005596716 |
| Address | Dag Hammarskjolds Vag 52a |
| City | Uppsala |
| Country | Sweden |
| Fiscal year | 2018 |
| Inspection end date | Jul 12, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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