FDA inspection
Jones Medical Instrument Co.: FDA inspection ending May 18, 2005
FDA inspection 380531 · No Action Indicated (NAI) · Oak Brook, IL
Key facts
| Inspection ID | 380531 |
|---|---|
| Firm | Jones Medical Instrument Co. |
| FEI number | 1416588 |
| Address | 200 Windsor Dr |
| City | Oak Brook |
| State | IL |
| ZIP | 60523-1507 |
| Fiscal year | 2005 |
| Inspection end date | May 18, 2005 |
| 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