Jones Medical Instrument Co.
Jones Medical Instrument Co. has 0 FDA recalls, 6 inspections, 2 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Oct 15, 2026 · NAI
- Latest 510(k)
- Aug 20, 1981
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 2 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 6 | Nov 11, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Oct 15, 2026 | Oak Brook, IL | Devices | No Action Indicated (NAI) | 1416588 |
| May 21, 2025 | Oak Brook, IL | Devices | No Action Indicated (NAI) | 1416588 |
| Sep 19, 2017 | Oak Brook, IL | Devices | No Action Indicated (NAI) | 1416588 |
| Nov 13, 2014 | Oak Brook, IL | Devices | Voluntary Action Indicated (VAI) | 1416588 |
| Oct 9, 2012 | Oak Brook, IL | Devices | No Action Indicated (NAI) | 1416588 |
| Mar 26, 2010 | Oak Brook, IL | Devices | No Action Indicated (NAI) | 1416588 |
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 1416588 | Oak Brook, IL | 6 | Oct 15, 2026 |