# Materialise N.V. – FDA Inspection, Mar 13, 2025

Source: https://www.keypedia.com/records/fda_inspections/materialise-nv/59574c78-1c2a-41dc-9422-a5538b73845c
Source feed: FDA_Inspections

> FDA inspection 1264936 of Materialise N.V., March 13, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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

## Related Documents

- FDA Inspection 1003668 - 2017-02-02
- [FDA Inspection 868332 - 2014-02-06](https://www.keypedia.com/records/fda_inspections/materialise-nv/57111e03-201d-4233-83ec-5900976a6592)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

Company: https://www.keypedia.com/companies/materialise-nv/2a11f5c8-845b-4917-9ac6-c5dbfb216ec6

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