FDA Inspection 1003668 — Materialise N.V.
The FDA completed an inspection of Materialise N.V. on February 2, 2017 in Leuven. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 2, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Leuven (Belgium)