FDA Inspection 1022539 — Materialise USA LLC
The FDA completed an inspection of Materialise USA LLC on August 1, 2017 in Plymouth, MI. 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
- August 1, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Plymouth, MI (United States)