FDA Inspection 859893 — Lumitex Medical Devices Inc
The FDA completed an inspection of Lumitex Medical Devices Inc on December 26, 2013 in Brecksville, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- December 26, 2013
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Brecksville, OH (United States)