FDA Inspection 1096551 - IQ PRODUCTS B.V. - July 17, 2019

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Record Details

This FDA Inspection record concerns IQ PRODUCTS B.V., with an inspection on July 17, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: IQ PRODUCTS B.V.
Inspection Date: July 17, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 32470abb-e967-483f-8b3a-b20bbdda079b

Violation Codes3

21 CFR 820.100(a)21 CFR 820.20(a)21 CFR 820.50(b)

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