FDA Inspection
Materialise N.V.Materialise N.V. – FDA Inspection, Feb 6, 2014
Record Details
This FDA Inspection record concerns Materialise N.V., with an inspection on February 6, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Materialise N.V.
- Inspection Date
- February 6, 2014
- Product Type
- Devices
View Company Profile
ID · 57111e03-201d-4233-83ec-5900976a6592
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 868332
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.198(e)Records of complaint investigation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Materialise N.V.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| March 13, 2025 | VAI | Office of Inspections and Investigations | Compliance: Medical Devices |
| February 2, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Materialise N.V.
- FDA Inspection 1264936 - 2025-03-13
- FDA Inspection 1003668 - 2017-02-02
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.