FDA inspection
Specialty Medical Products: FDA inspection ending Sep 25, 2007
FDA inspection 489516 · No Action Indicated (NAI) · N Salt Lake, UT
Key facts
| Inspection ID | 489516 |
|---|---|
| Firm | Specialty Medical Products |
| FEI number | 1721432 |
| Address | 101 North 700 West |
| City | N Salt Lake |
| State | UT |
| ZIP | 84010 |
| Fiscal year | 2007 |
| Inspection end date | Sep 25, 2007 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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