FDA EIR - Luminex Corporation - January 20, 2023

FDA EIR for Luminex Corporation on January 20, 2023. Product: devices. Access full analysis and detailed observations.

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Record Summary

FDA EIR for Luminex Corporation on January 20, 2023. Product: devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.198

21 CFR 820.30

21 CFR 820.100

21 CFR 803

21 CFR 820.50

21 CFR 803.17

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Record Information

Company

Luminex Corporation

Inspection Date

January 20, 2023

Product Type

devices

Office

Office of Medical Device and Radiological Health Division II

People

ID: da1d5c99-6d34-4f55-9d5f-57544e9bef7a

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