FDA Inspection 1056630 — Biocomposites GmbH (Former ARTOSS GmbH)
The FDA completed an inspection of Biocomposites GmbH (Former ARTOSS GmbH) on Apr 26, 2018 in Rostock. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Apr 26, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Rostock (Germany)