# FDA Inspection 958073 - Luminex Corporation - November 18, 2015

Source: https://www.keypedia.com/records/fda_inspections/luminex-corporation/668caa88-ab43-442f-9ba7-cd8a35dcd033
Source feed: FDA_Inspections

> FDA Inspection 958073 for Luminex Corporation on November 18, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 958073
- Company Name: Luminex Corporation
- Inspection Date: 2015-11-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/luminex-corporation/55525767-0124-4f84-8e09-0a8d7b03947e

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