FDA Inspection 730676 — Lumitex Medical Devices Inc
The FDA completed an inspection of Lumitex Medical Devices Inc on Jun 22, 2011 in Brecksville, OH. 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 22, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Brecksville, OH (United States)