FDA Inspection
Artivion, IncArtivion, Inc – FDA Inspection, Nov 23, 2010
Record Details
This FDA Inspection record concerns Artivion, Inc, with an inspection on November 23, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Artivion, Inc
- Inspection Date
- November 23, 2010
- Product Type
- Devices
View Company Profile
ID · 23788ff4-5d16-4bdc-888e-32a8a1a56404
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 699094
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
Other FDA inspections of Artivion, Inc
14| Date | Classification | Office | Project area |
|---|---|---|---|
| September 15, 2026 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 22, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 29, 2023 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 31, 2023 | VAI | Atlanta District Office | |
| January 20, 2022 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Artivion, Inc
- FDA Inspection 1337058 - 2026-09-15
- FDA Inspection 1237253 - 2024-03-22
- FDA Inspection 1218273 - 2023-08-29
- FDA Inspection 1201327 - 2023-03-31
- FDA Inspection 1161220 - 2022-01-20
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