Inspection classificationInspection ended September 15, 2026
FDA inspection of Artivion, Inc: NAI
No action indicated
FDA classified an inspection of Artivion, Inc in Kennesaw, GA as NAI (no action indicated). The inspection ended on September 15, 2026. Product type: Biologics.
On the record
- Establishment
- Artivion, Inc
- Location
- Kennesaw, GA
- Classification
- NAI · No action indicated
- Inspection ended
- 2026-09-15
- Product type
- Biologics
- Fiscal year
- FY2026
- FDA establishment identifier (FEI)
- 3001451326
- Source
- FDA Data Dashboard ↗
The full record
An account shows the project areas inspected and whether citations were posted.
What an inspection classification is
After an inspection FDA classifies the outcome. NAI (no action indicated): no objectionable conditions were found, or none that justify further action. VAI (voluntary action indicated): objectionable conditions were found, but the agency is not prepared to take or recommend regulatory action. OAI (official action indicated): regulatory or administrative action is recommended.
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From FDA Data Dashboard; FDA posts a classification after its review, which can be months after the inspection ended. The record may have changed since it was read.
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