FDA inspection
Specialty Medical Products: FDA inspection ending Feb 17, 2012
FDA inspection 768265 · Voluntary Action Indicated (VAI) · N Salt Lake, UT
Key facts
| Inspection ID | 768265 |
|---|---|
| Firm | Specialty Medical Products |
| FEI number | 1721432 |
| Address | 101 North 700 West |
| City | N Salt Lake |
| State | UT |
| ZIP | 84010 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Feb 17, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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