# Luminex Corporation – FDA Inspection, Oct 22, 2021

Source: https://www.keypedia.com/records/fda_inspections/luminex-corporation/baa929dc-d140-453f-9c94-b31c3d1d1283
Source feed: FDA_Inspections

> FDA inspection 1155192 of Luminex Corporation, October 22, 2021. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 806 and 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1155192
- Company Name: Luminex Corporation
- Inspection Date: 2021-10-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1195245 - 2023-01-20](https://www.keypedia.com/records/fda_inspections/luminex-corporation/eda149eb-a097-4c60-a3ab-322da99c171b)
- [FDA Inspection 1117864 - 2020-02-14](https://www.keypedia.com/records/fda_inspections/luminex-corporation/a4749b2c-587c-4405-9d71-c52ce0d92a82)
- FDA Inspection 1005213 - 2017-03-17
- [FDA Inspection 958073 - 2015-11-18](https://www.keypedia.com/records/fda_inspections/luminex-corporation/448c2877-4470-4d74-9129-4d0d817c3161)
- [FDA Inspection 874256 - 2014-04-04](https://www.keypedia.com/records/fda_inspections/luminex-corporation/b644e37c-a55d-4913-9094-d4050f8a0c76)

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
