FDA Inspection 981339 — Lightbody Medical Technologies Inc
The FDA completed an inspection of Lightbody Medical Technologies Inc on Aug 22, 2016 in Burr Ridge, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 22, 2016
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Burr Ridge, IL (United States)