# Freudenberg Medical Europe GmbH – FDA Inspection, Oct 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 of Freudenberg Medical Europe GmbH, October 30, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 2

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