FDA Inspection 1000739 - Euro Diagnostica AB - January 19, 2017

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Record Details

This FDA Inspection record concerns Euro Diagnostica AB, with an inspection on January 19, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Euro Diagnostica AB
Inspection Date: January 19, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ba3afce9-7bb2-4e20-9176-09831eab25a2

Violation Codes7

21 CFR 803.17(a)(3)21 CFR 806.20(b)(4)21 CFR 820.100(b)21 CFR 820.198(a)21 CFR 820.2221 CFR 820.30(e)21 CFR 820.30(f)

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