FDA Inspection 592915 — Lightbody Medical Technologies Inc
The FDA completed an inspection of Lightbody Medical Technologies Inc on Jun 17, 2009 in Burr Ridge, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jun 17, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Burr Ridge, IL (United States)