FDA inspection
Fischer Imaging Corporation: FDA inspection ending Sep 25, 2001
FDA inspection 90296 · Voluntary Action Indicated (VAI) · Broomfield, CO
Key facts
| Inspection ID | 90296 |
|---|---|
| Firm | Fischer Imaging Corporation |
| FEI number | 1418957 |
| Address | 370 Interlocken Blvd Fl 4th |
| City | Broomfield |
| State | CO |
| ZIP | 80021-8009 |
| Fiscal year | 2001 |
| Inspection end date | Sep 25, 2001 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med 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