FDA Inspection 561479 — Luminex Corporation
The FDA completed an inspection of Luminex Corporation on Feb 9, 2009 in Austin, TX. 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
- Feb 9, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Austin, TX (United States)