FDA inspection
Perseon Corporation: FDA inspection ending Nov 30, 2016
FDA inspection 993576 · No Action Indicated (NAI) · Salt Lake City, UT
Key facts
| Inspection ID | 993576 |
|---|---|
| Firm | Perseon Corporation |
| FEI number | 1719106 |
| Address | 391 S Chipeta Way Ste F |
| City | Salt Lake City |
| State | UT |
| ZIP | 84108 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Nov 30, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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