FDA Inspection 1074723 - Kitron AB - December 13, 2018

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Record Details

This FDA Inspection record concerns Kitron AB, with an inspection on December 13, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Kitron AB
Inspection Date: December 13, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 50982007-241d-4747-9f3f-3a11454737e4

Violation Codes9

21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.5021 CFR 820.75(a)21 CFR 820.80(a)21 CFR 820.90(a)

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