# FDA Inspection 1289226 - Freudenberg Medical Europe GmbH - October 30, 2025

Source: https://www.keypedia.com/records/fda_inspections/freudenberg-medical-europe-gmbh/cfe53d24-9d33-460b-833b-3aeb0ed59a31
Source feed: FDA_Inspections

> FDA Inspection 1289226 for Freudenberg Medical Europe GmbH on October 30, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1289226
- Company Name: Freudenberg Medical Europe GmbH
- Inspection Date: 2025-10-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations

Company: https://www.keypedia.com/companies/freudenberg-medical-europe-gmbh/ba402628-9028-40dd-8699-5730769e260d

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8