# FDA Inspection 1264936 - Materialise N.V. - March 13, 2025

Source: https://www.keypedia.com/records/fda_inspections/materialise-nv/3a8f621d-0583-4bf6-8ba7-4401ee49e455
Source feed: FDA_Inspections

> FDA Inspection 1264936 for Materialise N.V. on March 13, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1264936
- Company Name: Materialise N.V.
- Inspection Date: 2025-03-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1264936 - 2025-03-13](https://www.keypedia.com/records/fda_inspections/materialise-nv/59574c78-1c2a-41dc-9422-a5538b73845c)
- [FDA Inspection 1264936 - 2025-03-13](https://www.keypedia.com/records/fda_inspections/materialise-nv/97daf63d-4bec-427a-9c90-b5fdc2978950)
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Company: https://www.keypedia.com/companies/materialise-nv/2a11f5c8-845b-4917-9ac6-c5dbfb216ec6

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