FDA Inspection 911848 - Artegraft, Inc. - January 28, 2015

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Record Details

This FDA Inspection record concerns Artegraft, Inc., with an inspection on January 28, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Artegraft, Inc.
Inspection Date: January 28, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 924731d1-b0b3-41a9-bcba-8967e5a1076f

Violation Codes5

21 CFR 820.100(a)21 CFR 820.18121 CFR 820.18421 CFR 820.250(b)21 CFR 820.75(a)

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