# Artivion, Inc – FDA Inspection, Mar 19, 2014

Source: https://www.keypedia.com/records/fda_inspections/artivion-inc/e9a1ca0a-2078-48e8-8c20-d367cb7105a7
Source feed: FDA_Inspections

> FDA inspection 870540 of Artivion, Inc, March 19, 2014. Classification: Official Action Indicated (OAI). 16 citations under 21 CFR parts 820 and 1271. 14 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 870540
- Company Name: Artivion, Inc
- Inspection Date: 2014-03-19
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 16

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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