FDA inspection
OrthoPro LLC: FDA inspection ending Jun 3, 2008
FDA inspection 523189 · Voluntary Action Indicated (VAI) · Salt Lake City, UT
Key facts
| Inspection ID | 523189 |
|---|---|
| Firm | OrthoPro LLC |
| FEI number | 3005252592 |
| Address | 3939 S Wasatch Blvd Ste 19 |
| City | Salt Lake City |
| State | UT |
| ZIP | 84124-2216 |
| Fiscal year | 2008 |
| Inspection end date | Jun 3, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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