# FDA Inspection 561479 - Luminex Corporation - February 09, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/luminex-corporation/d14c10bd-3385-4028-8a61-5e5259ab5a89
Source feed: FDA_Inspections

> FDA Inspection 561479 for Luminex Corporation on February 09, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 561479
- Company Name: Luminex Corporation
- Inspection Date: 2009-02-09
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/luminex-corporation/89e2a70e-d1fc-4c47-b6a0-5ccfff829ecb

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7