FDA Inspection 1232568 — Axogen Corporation

Axogen Corporation — FEI 3017860045

The FDA completed an inspection of Axogen Corporation on Feb 29, 2024 in Tampa, FL. 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
Feb 29, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Tampa, FL (United States)