FDA Inspection 843981 - Greiner Bio-One North America, Inc. - July 24, 2013

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Record Details

This FDA Inspection record concerns Greiner Bio-One North America, Inc., with an inspection on July 24, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Greiner Bio-One North America, Inc.
Inspection Date: July 24, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b1077252-af18-4942-ad6a-169e39e22045

Violation Codes8

21 CFR 820.20(c)21 CFR 820.30(f)21 CFR 820.70(a)21 CFR 820.75(a)21 CFR 820.75(b)(2)21 CFR 820.75(c)21 CFR 820.80(d)21 CFR 820.90(a)

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