FDA Inspection 833228 - Artivion, Inc - May 23, 2013

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Record Details

This FDA Inspection record concerns Artivion, Inc, with an inspection on May 23, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Artivion, Inc
Inspection Date: May 23, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6768f78d-0444-47c6-a60d-4f6ddca17df2

Violation Codes10

21 CFR 1002.1321 CFR 1003.10(a)21 CFR 1040.10(h)(1)(vi)21 CFR 1040.10(h)(2)(ii)21 CFR 803.50(a)(2)21 CFR 806.10(a)(1)21 CFR 820.198(c)21 CFR 820.2221 CFR 820.72(a)21 CFR 820.80(c)

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