FDA inspection
G. Dundas Co Inc: FDA inspection ending Aug 8, 2019
FDA inspection 1101332 · Voluntary Action Indicated (VAI) · Black Diamond, WA
Key facts
| Inspection ID | 1101332 |
|---|---|
| Firm | G. Dundas Co Inc |
| FEI number | 3019855 |
| Address | 24301 Roberts Dr |
| City | Black Diamond |
| State | WA |
| ZIP | 98010 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Aug 8, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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