Precision One Medical, Inc.
Precision One Medical, Inc. has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Aug 26, 2025 · NAI
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 4, 2026 (checked Nov 8, 2026, unchanged) | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 8 | Nov 9, 2026 | Newest record Oct 28, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Aug 26, 2025 | Hoover, AL | Devices | No Action Indicated (NAI) | 3017980266 |
| Jun 12, 2023 | Oceanside, CA | Devices | No Action Indicated (NAI) | 3009201148 |
| Sep 28, 2015 | Oceanside, CA | Devices | No Action Indicated (NAI) | 3009201148 |
| Aug 28, 2015 | Oceanside, CA | Devices | Voluntary Action Indicated (VAI) | 3009201148 |
| Dec 9, 2013 | Oceanside, CA | Devices | No Action Indicated (NAI) | 3009201148 |
| Sep 18, 2013 | Oceanside, CA | Devices | No Action Indicated (NAI) | 3009201148 |
| Oct 28, 2011 | Oceanside, CA | Devices | Voluntary Action Indicated (VAI) | 3009201148 |
| Oct 26, 2011 | Oceanside, CA | Devices | No Action Indicated (NAI) | 3009201148 |
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3017980266 | Hoover, AL | 1 | Aug 26, 2025 |
| FEI 3009201148 | Oceanside, CA | 7 | Jun 12, 2023 |