FDA inspection
Axis-Shield Diagnostics, Ltd.: FDA inspection ending Oct 25, 2018
FDA inspection 1072250 · Voluntary Action Indicated (VAI) · Dundee
Key facts
| Inspection ID | 1072250 |
|---|---|
| Firm | Axis-Shield Diagnostics, Ltd. |
| FEI number | 3002808140 |
| Address | 17 Luna Place, Dnd |
| City | Dundee |
| Country | United Kingdom |
| Fiscal year | 2019 |
| Inspection end date | Oct 25, 2018 |
| 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