# FDA Inspection 803320 - Artivion, Inc - October 16, 2012

Source: https://www.keypedia.com/records/fda_inspections/artivion-inc/d409705b-1909-44cc-81ae-0dad0fa479eb
Source feed: FDA_Inspections

> FDA Inspection 803320 for Artivion, Inc on October 16, 2012. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803320
- Company Name: Artivion, Inc
- Inspection Date: 2012-10-16
- Classification: Official Action Indicated (OAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

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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-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d