Oxus, Inc.
Oxus, Inc. has 0 FDA recalls, 4 inspections, 2 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Oct 10, 2019 · NAI
- Latest 510(k)
- May 31, 2023
Reviewing Oxus, Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Or get Oxus, Inc.'s full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 2 | Oct 4, 2026 | Not stated | Current |
| Inspections | 4 | Oct 26, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Oct 10, 2019 | Auburn Hills, MI | Devices | No Action Indicated (NAI) | 3008841036 |
| Jan 19, 2016 | Auburn Hills, MI | Devices | Voluntary Action Indicated (VAI) | 3008841036 |
| Sep 20, 2013 | Auburn Hills, MI | Devices | No Action Indicated (NAI) | 3008841036 |
| Aug 1, 2011 | Auburn Hills, MI | Devices | Voluntary Action Indicated (VAI) | 3008841036 |