FDA Inspection 1280511 - Vygon GmbH & Co. KG - September 04, 2025

Record Details

This FDA Inspection record concerns Vygon GmbH & Co. KG, with an inspection on September 4, 2025, issued by the Center for Devices and Radiological Health, covering devices.

Company: Vygon GmbH & Co. KG
Inspection Date: September 4, 2025
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · dd1f1759-ee15-4f90-9385-e353d3ed66c8

Violation Codes2

21 CFR 820.100(a)21 CFR 820.198(a)

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