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FDA Inspection 665220 — Artivion, Inc

Artivion, Inc — FEI 3001451326

The FDA completed an inspection of Artivion, Inc on April 21, 2010 in Kennesaw, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 21, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Kennesaw, GA (United States)

Facility

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Recent compliance actions

FDA data resources