# FDA Inspection 833228 - Artivion, Inc - May 23, 2013

Source: https://www.keypedia.com/records/fda_inspections/artivion-inc/d39b687c-c6eb-42b2-b6e3-b88ddbbf453b
Source feed: FDA_Inspections

> FDA Inspection 833228 for Artivion, Inc on May 23, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 833228
- Company Name: Artivion, Inc
- Inspection Date: 2013-05-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- 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