FDA Inspection 583137 - Stryker Corporation - May 14, 2009

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Record Details

This FDA Inspection record concerns Stryker Corporation, with an inspection on May 14, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Stryker Corporation
Inspection Date: May 14, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 69d21025-1eec-4c2d-8630-92ab1538a1ad

Violation Codes10

21 CFR 803.50(a)(2)21 CFR 820.198(a)21 CFR 820.25(b)21 CFR 820.250(b)21 CFR 820.30(g)21 CFR 820.50(a)(1)21 CFR 820.75(a)21 CFR 820.75(b)(1)21 CFR 820.90(a)21 CFR 820.90(b)(2)

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