FDA Inspection 1315568 — Axogen Corporation

Axogen Corporation — FEI 3012085771

The FDA completed an inspection of Axogen Corporation on April 9, 2026 in Dayton, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 9, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Dayton, OH (United States)