# Axogen Corporation - Inspection Records

Source: https://www.globalkeysolutions.net/companies/axogen-corporation/c1a3a1ba-57e3-4747-b670-8018198f0309

> Inspection records and compliance data for Axogen Corporation in Burleson, Texas. Access full analysis and detailed observations.

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## Details

- Name: Axogen Corporation
- FEI Number: 3011006318
- City: Burleson
- State: Texas
- Country Name: United States
- Address Line 1: 300 Boone Rd Ste A3
- Zip Code: 76028

## Related Documents

- [FDA Inspection 1298590 - Axogen Corporation - 2026-01-08](https://www.globalkeysolutions.net/records/fda_inspections/axogen-corporation/e55e94f9-e171-49df-acbe-d468ddee1c33) — source: FDA, date: January 8, 2026
- [FDA Inspection 1298590 - Axogen Corporation - 2026-01-08](https://www.globalkeysolutions.net/records/fda_inspections/axogen-corporation/8f2b66e1-c593-4c93-ae70-fde78de1c0a5) — classification: No Action Indicated (NAI), source: FDA, date: January 8, 2026
- [FDA Inspection 1275112 - Axogen Corporation - 2025-06-19](https://www.globalkeysolutions.net/records/fda_inspections/axogen-corporation/f4ae9eb6-cb40-4c95-b2cc-c695779c02b9) — source: FDA, date: June 19, 2025
- [FDA Inspection 1177562 - Axogen Corporation - 2022-07-28](https://www.globalkeysolutions.net/records/fda_inspections/axogen-corporation/9c7e1070-8682-48b1-a9a3-6aaf52d34e1f) — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2022
- [FDA Inspection 1177562 - Axogen Corporation - 2022-07-28](https://www.globalkeysolutions.net/records/fda_inspections/axogen-corporation/7f8207b3-ab62-4808-bc34-8f8c876ad843) — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2022
- [FDA Inspection 1072238 - Axogen Corporation - 2018-11-20](https://www.globalkeysolutions.net/records/fda_inspections/axogen-corporation/6c574dbc-677c-4b2f-ae65-d7b0959d53d0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 20, 2018
- [FDA Inspection 946545 - Axogen Corporation - 2015-10-13](https://www.globalkeysolutions.net/records/fda_inspections/axogen-corporation/eb8a3569-4c53-42c7-b8ab-12990b1954b0) — classification: No Action Indicated (NAI), source: FDA, date: October 13, 2015

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