# FDA Inspection 1161220 - Artivion, Inc - January 20, 2022

Source: https://www.keypedia.com/records/fda_inspections/artivion-inc/27127e6f-da06-4a38-95c3-824e1e923ebd
Source feed: FDA_Inspections

> FDA Inspection 1161220 for Artivion, Inc on January 20, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1161220
- Company Name: Artivion, Inc
- Inspection Date: 2022-01-20
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/artivion-inc/484ce438-d451-4d95-ab4c-726a2dc02c92

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