Rechon Life Science AB
Rechon Life Science AB has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 1 compliance action on record.
- Latest inspection
- Sep 6, 2024 · OAI
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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 | 7 | Nov 8, 2026 | Newest record Oct 28, 2026 | Current |
| Compliance actions | 1 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Sep 6, 2024 | Limhamn, Sweden | Drugs | Official Action Indicated (OAI) | 3002806978 |
| Nov 27, 2019 | Limhamn, Sweden | Drugs | Voluntary Action Indicated (VAI) | 3002806978 |
| Jun 29, 2018 | Limhamn, Sweden | Drugs | Voluntary Action Indicated (VAI) | 3002806978 |
| Jun 2, 2016 | Limhamn, Sweden | Devices | No Action Indicated (NAI) | 3002806978 |
| Apr 29, 2016 | Limhamn, Sweden | Drugs | Voluntary Action Indicated (VAI) | 3002806978 |
| Mar 21, 2014 | Limhamn, Sweden | Drugs | Voluntary Action Indicated (VAI) | 3002806978 |
| Sep 16, 2011 | Limhamn, Sweden | Drugs | Voluntary Action Indicated (VAI) | 3002806978 |
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3002806978 | Limhamn, Sweden | 7 | Sep 6, 2024 |