FDA Inspection 1252370 — Biocomposites GmbH (Former ARTOSS GmbH)

Biocomposites GmbH (Former ARTOSS GmbH) — FEI 3011483489

The FDA completed an inspection of Biocomposites GmbH (Former ARTOSS GmbH) on Sep 19, 2024 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
Sep 19, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Rostock (Germany)