FDA inspection
G. Dundas Co Inc: FDA inspection ending Aug 10, 2005
FDA inspection 390479 · Voluntary Action Indicated (VAI) · Black Diamond, WA
Key facts
| Inspection ID | 390479 |
|---|---|
| Firm | G. Dundas Co Inc |
| FEI number | 3019855 |
| Address | 24301 Roberts Dr |
| City | Black Diamond |
| State | WA |
| ZIP | 98010-9219 |
| Fiscal year | 2005 |
| Inspection end date | Aug 10, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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