# AxoGen Corporation – FDA Inspection, Feb 8, 2018

Source: https://www.keypedia.com/records/fda_inspections/axogen-corporation/76a73d00-71a5-4ef7-be89-665fff16aa4d
Source feed: FDA_Inspections

> FDA inspection 1040447 of AxoGen Corporation, February 08, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1040447
- Company Name: AxoGen Corporation
- Inspection Date: 2018-02-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1214536 - 2023-08-04

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/barbara-t-carmichael/4c451805-e327-450d-b2e5-48a40f6232fe)
- Issuing Officer

Company: https://www.keypedia.com/companies/axogen-corporation/a43af3b1-a05c-440e-930c-a685952a6d70

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7