FDA Inspection 1000208 — Lumitex Medical Devices Inc
The FDA completed an inspection of Lumitex Medical Devices Inc on Jan 9, 2017 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
- Jan 9, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Brecksville, OH (United States)