FDA inspection
Artivion, Inc: FDA inspection ending Jan 20, 2022
FDA inspection 1161220 · No Action Indicated (NAI) · Kennesaw, GA
Key facts
| Inspection ID | 1161220 |
|---|---|
| Firm | Artivion, Inc |
| FEI number | 3001451326 |
| Address | 1655 Roberts Blvd Nw |
| City | Kennesaw |
| State | GA |
| ZIP | 30144 |
| Country | United States |
| Fiscal year | 2022 |
| Inspection end date | Jan 20, 2022 |
| Classification | No Action Indicated (NAI) |
| Project area | Bioresearch Monitoring |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data