FDA inspection
Jones Medical Instrument Co.: FDA inspection ending Aug 3, 2007
FDA inspection 482282 · Voluntary Action Indicated (VAI) · Oak Brook, IL
Key facts
| Inspection ID | 482282 |
|---|---|
| Firm | Jones Medical Instrument Co. |
| FEI number | 1416588 |
| Address | 200 Windsor Dr |
| City | Oak Brook |
| State | IL |
| ZIP | 60523-1507 |
| Fiscal year | 2007 |
| Inspection end date | Aug 3, 2007 |
| 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