Lightbody Medical Technologies Inc
Lightbody Medical Technologies Inc has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Aug 27, 2025 · VAI
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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 | 6 | 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 27, 2025 | Burr Ridge, IL | Biologics | Voluntary Action Indicated (VAI) | 3007048062 |
| Jun 4, 2019 | Burr Ridge, IL | Biologics | No Action Indicated (NAI) | 3007048062 |
| Aug 22, 2016 | Burr Ridge, IL | Biologics | No Action Indicated (NAI) | 3007048062 |
| Jul 24, 2014 | Burr Ridge, IL | Biologics | No Action Indicated (NAI) | 3007048062 |
| Nov 2, 2011 | Burr Ridge, IL | Biologics | No Action Indicated (NAI) | 3007048062 |
| Jun 17, 2009 | Burr Ridge, IL | Devices | No Action Indicated (NAI) | 3007048062 |
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3007048062 | Burr Ridge, IL | 6 | Aug 27, 2025 |