# FDA Inspection 1218273 - Artivion, Inc - August 29, 2023

Source: https://www.keypedia.com/records/fda_inspections/artivion-inc/1f20a3d0-a4e8-4e5b-9c1d-65bdf4a3042e
Source feed: FDA_Inspections

> FDA Inspection 1218273 for Artivion, Inc on August 29, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1218273
- Company Name: Artivion, Inc
- Inspection Date: 2023-08-29
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- 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