FDA inspection
Stereotaxis Inc: FDA inspection ending Feb 15, 2008
FDA inspection 506243 · Voluntary Action Indicated (VAI) · Saint Louis, MO
Key facts
| Inspection ID | 506243 |
|---|---|
| Firm | Stereotaxis Inc |
| FEI number | 3003084417 |
| Address | 710 N Tucker Blvd Ste 110 |
| City | Saint Louis |
| State | MO |
| ZIP | 63101-1150 |
| Fiscal year | 2008 |
| Inspection end date | Feb 15, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: 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