# Artivion, Inc - Inspection Records

Source: https://www.keypedia.com/companies/artivion-inc/484ce438-d451-4d95-ab4c-726a2dc02c92

> Inspection records and compliance data for Artivion, Inc in Kennesaw, Georgia. Access full analysis and detailed observations.

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## Details

- Name: Artivion, Inc
- FEI Number: 3001451326
- City: Kennesaw
- State: Georgia
- Country Name: United States
- Address Line 1: 1655 Roberts Blvd Nw
- Zip Code: 30144
- Facility Type: Human Tissue Processor/Medical Device Manu

## Related Documents

- [FDA Inspection 1237253 - Artivion, Inc - 2024-03-22](https://www.keypedia.com/records/fda_inspections/artivion-inc/a898e44b-aeac-4275-b1a5-7391da2d4cb4) — classification: No Action Indicated (NAI), source: FDA, date: March 22, 2024
- [FDA Inspection 1218273 - Artivion, Inc - 2023-08-29](https://www.keypedia.com/records/fda_inspections/artivion-inc/e6a36b91-da57-4ad6-b985-48246805dff8) — classification: No Action Indicated (NAI), source: FDA, date: August 29, 2023
- [FDA Inspection 1218273 - Artivion, Inc - 2023-08-29](https://www.keypedia.com/records/fda_inspections/artivion-inc/1f20a3d0-a4e8-4e5b-9c1d-65bdf4a3042e) — classification: No Action Indicated (NAI), source: FDA, date: August 29, 2023
- [483 - Artivion, Inc - 2023-03-31](https://www.keypedia.com/records/483/artivion-inc/e75a540f-30c1-401b-9ee8-ee4cdbf56e04) — source: FDA, date: March 31, 2023
- [FDA Inspection 1161220 - Artivion, Inc - 2022-01-20](https://www.keypedia.com/records/fda_inspections/artivion-inc/27127e6f-da06-4a38-95c3-824e1e923ebd) — classification: No Action Indicated (NAI), source: FDA, date: January 20, 2022
- [483 - Artivion, Inc - 2018-08-08](https://www.keypedia.com/records/483/artivion-inc/ac594da7-b44a-47cc-a976-a6fea3066a5c) — source: FDA, date: August 8, 2018
- [FDA Inspection 1061747 - Artivion, Inc - 2018-08-08](https://www.keypedia.com/records/fda_inspections/artivion-inc/f14569d7-1fd5-4d71-aea4-4ff76d24898d) — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2018
- [FDA Inspection 1061747 - Artivion, Inc - 2018-08-08](https://www.keypedia.com/records/fda_inspections/artivion-inc/b76377e9-c7ab-4bd8-96a4-efc2dd7d9fe8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 8, 2018
- [FDA Inspection 1061747 - Artivion, Inc - 2018-08-08](https://www.keypedia.com/records/fda_inspections/artivion-inc/fad52078-6831-4821-a5d1-afaf123164ca) — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2018
- [FDA Inspection 1061747 - Artivion, Inc - 2018-08-08](https://www.keypedia.com/records/fda_inspections/artivion-inc/6df73d95-b4c0-4de8-926f-5409b3da5f27) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 8, 2018
- [FDA Inspection 917957 - Artivion, Inc - 2015-03-16](https://www.keypedia.com/records/fda_inspections/artivion-inc/a88f6bff-dfbe-45cf-b9bf-80a9c222badf) — classification: No Action Indicated (NAI), source: FDA, date: March 16, 2015
- [FDA Inspection 917957 - Artivion, Inc - 2015-03-16](https://www.keypedia.com/records/fda_inspections/artivion-inc/76a7e126-c08a-4fbf-b44b-d5be3630ba9d) — classification: No Action Indicated (NAI), source: FDA, date: March 16, 2015
- [483 - Artivion, Inc - 2003-02-14](https://www.keypedia.com/records/483/artivion-inc/03061550-2828-460f-9834-9b7cce079bd2) — source: FDA, date: February 14, 2003

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