FDA Inspection 981779 - Stryker Corporation - August 25, 2016

FDA Inspection 981779 for Stryker Corporation on August 25, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 981779 for Stryker Corporation on August 25, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Stryker Corporation

Inspection Date

August 25, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fb435a32-58b6-44ee-ae49-a81e9525d4ea

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