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FDA Inspection 1218273 — Artivion, Inc

Artivion, Inc — FEI 3001451326

The FDA completed an inspection of Artivion, Inc on August 29, 2023 in Kennesaw, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 29, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Kennesaw, GA (United States)

Facility

Other inspections at this facility

  • 1237253 (NAI Fri Mar 22 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1161220 (NAI Thu Jan 20 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1061747 (NAI Wed Aug 08 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 917957 (NAI Mon Mar 16 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 870540 (OAI Wed Mar 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources