Inbody Co., Ltd.
Inbody Co., Ltd. has 0 FDA recalls, 2 inspections, 4 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Aug 10, 2017 · NAI
- Latest 510(k)
- Aug 2, 2023
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 4 | Oct 4, 2026 | Not stated | Current |
| Inspections | 2 | Oct 23, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Aug 10, 2017 | Cheonan, Korea (The Republic Of) | Devices | No Action Indicated (NAI) | 3003074886 |
| Aug 10, 2017 | Seoul, Korea (The Republic Of) | Devices | No Action Indicated (NAI) | 3011541022 |