FDA inspection
Barton-Carey Medical Products Inc: FDA inspection ending Aug 16, 2002
FDA inspection 230694 · Voluntary Action Indicated (VAI) · Jellico, TN
Key facts
| Inspection ID | 230694 |
|---|---|
| Firm | Barton-Carey Medical Products Inc |
| FEI number | 3003070670 |
| Address | 460 5th St |
| City | Jellico |
| State | TN |
| ZIP | 37762-2504 |
| Fiscal year | 2002 |
| Inspection end date | Aug 16, 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