FDA inspection
Fischer Medical Technologies, Inc.: FDA inspection ending Jun 5, 2009
FDA inspection 587950 · Voluntary Action Indicated (VAI) · Wheat Ridge, CO
Key facts
| Inspection ID | 587950 |
|---|---|
| Firm | Fischer Medical Technologies, Inc. |
| FEI number | 3006188092 |
| Address | 3990 Youngfield St |
| City | Wheat Ridge |
| State | CO |
| ZIP | 80033 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Jun 5, 2009 |
| 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