FDA Inspection 806763 - Stryker Corporation - November 09, 2012

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Record Details

This FDA Inspection record concerns Stryker Corporation, with an inspection on November 9, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: Stryker Corporation
Inspection Date: November 9, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 29a6507f-9b68-4137-855e-f2f75e9ad7c3

Violation Codes6

21 CFR 803.50(a)(2)21 CFR 806.10(a)(1)21 CFR 820.30(g)21 CFR 820.30(i)21 CFR 820.50(a)(2)21 CFR 820.72(a)

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