FDA Inspection 1034752 - GAELTEC DEVICES LTD - December 07, 2017

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Record Details

This FDA Inspection record concerns GAELTEC DEVICES LTD, with an inspection on December 7, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: GAELTEC DEVICES LTD
Inspection Date: December 7, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5276249e-6ab7-419a-bd89-aa70230fe75b

Violation Codes5

21 CFR 820.100(a)21 CFR 820.18421 CFR 820.198(a)21 CFR 820.70(g)(1)21 CFR 820.75(a)

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