FDA inspection
KORR Medical Technologies, Inc.: FDA inspection ending May 10, 2014
FDA inspection 878261 · Voluntary Action Indicated (VAI) · Salt Lake City, UT
Key facts
| Inspection ID | 878261 |
|---|---|
| Firm | KORR Medical Technologies, Inc. |
| FEI number | 3002892786 |
| Address | 3487 W 2100 S Ste 300 |
| City | Salt Lake City |
| State | UT |
| ZIP | 84119 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | May 10, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 10–99 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