FDA Inspection 1279663 — Lightbody Medical Technologies Inc
The FDA completed an inspection of Lightbody Medical Technologies Inc on Aug 27, 2025 in Burr Ridge, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Biologics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Aug 27, 2025
- Fiscal Year
- 2025
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Burr Ridge, IL (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 12419 | 21 CFR 1271.265(a) | Evaluation--microorganisms, damage |