Nuvoair AB
Nuvoair AB has 0 FDA recalls, 1 inspection, 2 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Sep 22, 2022 · VAI
- Latest 510(k)
- Jan 18, 2024
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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 | 1 | Oct 27, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Sep 22, 2022 | Stockholm, Sweden | Devices | Voluntary Action Indicated (VAI) | 3013744763 |