# Artivion, Inc – FDA Inspection, Oct 16, 2012

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

> FDA inspection 803320 of Artivion, Inc, October 16, 2012. Classification: Official Action Indicated (OAI). 12 citations under 21 CFR parts 820 and 1271. 14 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 803320
- Company Name: Artivion, Inc
- Inspection Date: 2012-10-16
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Center: Biologics
- Office Name: Center for Biologics Evaluation and Research
- Citation Count: 12

## Related Documents

- FDA Inspection 1337058 - 2026-09-15
- FDA Inspection 1237253 - 2024-03-22
- FDA Inspection 1218273 - 2023-08-29
- [FDA Inspection 1201327 - 2023-03-31](https://www.keypedia.com/records/fda_inspections/artivion-inc/43b3a45d-ac3b-451b-9704-99bd2ea7baa3)
- FDA Inspection 1161220 - 2022-01-20

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