# Artivion, Inc – FDA Inspection, Nov 23, 2010

Source: https://www.keypedia.com/records/fda_inspections/artivion-inc/23788ff4-5d16-4bdc-888e-32a8a1a56404
Source feed: FDA_Inspections

> FDA inspection 699094 of Artivion, Inc, November 23, 2010. Classification: No Action Indicated (NAI). 14 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 699094
- Company Name: Artivion, Inc
- Inspection Date: 2010-11-23
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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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