FDA Inspection 1192014 - Kitron AB - November 10, 2022

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Record Details

This FDA Inspection record concerns Kitron AB, with an inspection on November 10, 2022, issued by the Center for Devices and Radiological Health, covering devices.

Company: Kitron AB
Inspection Date: November 10, 2022
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4bdd1d62-60c8-4c28-af86-f5ee91c60a86

Violation Codes4

21 CFR 820.198(a)21 CFR 820.25(b)21 CFR 820.5021 CFR 820.75(a)

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