FDA inspection
Sanders Medical Products Inc: FDA inspection ending Jan 10, 2002
FDA inspection 199820 · Voluntary Action Indicated (VAI) · Knoxville, TN
Key facts
| Inspection ID | 199820 |
|---|---|
| Firm | Sanders Medical Products Inc |
| FEI number | 3001237189 |
| Address | 520 Bearden Park Cir |
| City | Knoxville |
| State | TN |
| ZIP | 37919-7441 |
| Fiscal year | 2002 |
| Inspection end date | Jan 10, 2002 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None 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