FDA Inspection 1190791 - Vygon GmbH & Co. KG - November 10, 2022

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Record Details

This FDA Inspection record concerns Vygon GmbH & Co. KG, with an inspection on November 10, 2022, issued by the Center for Devices and Radiological Health, covering devices.

Company: Vygon GmbH & Co. KG
Inspection Date: November 10, 2022
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 8b337dcd-ec57-4f7c-acea-164256363054

Violation Codes3

21 CFR 820.100(b)21 CFR 820.198(c)21 CFR 820.25(b)

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