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

Source: https://www.globalkeysolutions.net/records/fda_inspections/vygon-gmbh-co-kg/dd1f1759-ee15-4f90-9385-e353d3ed66c8
Source feed: FDA_Inspections

> FDA Inspection 1280511 for Vygon GmbH & Co. KG on September 04, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280511
- Company Name: Vygon GmbH & Co. KG
- Inspection Date: 2025-09-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/vygon-gmbh-co-kg/d64f5fbf-9e9a-49bb-b9f2-599a21ffd75b

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7