FDA Inspection 919999 — Axogen Corporation

Axogen Corporation — FEI 3012085771

The FDA completed an inspection of Axogen Corporation on March 13, 2015 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
March 13, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Dayton, OH (United States)