# FDA Inspection 1061747 - Artivion, Inc - August 08, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/artivion-inc/fad52078-6831-4821-a5d1-afaf123164ca/
Source feed: FDA_Inspections

> FDA Inspection 1061747 for Artivion, Inc on August 08, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1061747
- Company Name: Artivion, Inc
- Inspection Date: 2018-08-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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