FDA Inspection 1069978 — Osseus Fusion Systems, LLC

Osseus Fusion Systems, LLC — FEI 3010531060

The FDA completed an inspection of Osseus Fusion Systems, LLC on Aug 24, 2018 in Dallas, TX. 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
Aug 24, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Dallas, TX (United States)