FDA Inspection 803320 - Artivion, Inc - October 16, 2012

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Record Details

This FDA Inspection record concerns Artivion, Inc, with an inspection on October 16, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: Artivion, Inc
Inspection Date: October 16, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4fe11cab-61c4-425d-bb9a-7d98f9697b41

Violation Codes10

21 CFR 1271.220(a)21 CFR 820.100(b)21 CFR 820.198(c)21 CFR 820.20(c)21 CFR 820.250(b)21 CFR 820.30(e)21 CFR 820.30(j)21 CFR 820.70(a)21 CFR 820.70(c)21 CFR 820.75(b)

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