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

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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 medical devices & rad health.

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

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ID · e1b2b77a-16c1-4e11-935a-c605112680d8

Violation Codes2

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

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