FDA Inspection 1106700 - MANDELAY KFT - October 17, 2019

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Record Details

This FDA Inspection record concerns MANDELAY KFT, with an inspection on October 17, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: MANDELAY KFT
Inspection Date: October 17, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0256b83a-ab32-470e-8a33-0bebca5719b4

Violation Codes4

21 CFR 820.120(b)21 CFR 820.198(a)21 CFR 820.30(a)21 CFR 820.70(c)

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