# Luminex Corporation – FDA Inspection, Jan 13, 2023

Source: https://www.keypedia.com/records/fda_inspections/luminex-corporation/e7244dbc-2e96-4f96-b26c-16fdeba4020b
Source feed: FDA_Inspections

> FDA inspection 1195233 of Luminex Corporation, January 13, 2023. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1195233
- Company Name: Luminex Corporation
- Inspection Date: 2023-01-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1117835 - 2020-02-14](https://www.keypedia.com/records/fda_inspections/luminex-corporation/fd97a76c-22aa-4ef5-ae12-f68ba116b9d9)
- [FDA Inspection 1079277 - 2018-04-06](https://www.keypedia.com/records/fda_inspections/luminex-corporation/65c698b5-c61f-4be6-8069-1b39f75b1ea8)
- FDA Inspection 768656 - 2012-02-15
- FDA Inspection 561479 - 2009-02-09

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nicholas-z-lu/17448aca-e316-424c-b7b2-88c8baffc359)

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

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