FDA Inspection 823160 - Neuropace Inc - March 05, 2013

FDA Inspection 823160 for Neuropace Inc on March 05, 2013. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 823160 for Neuropace Inc on March 05, 2013. Classification: No Action Indicated (NAI).

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Record Information

Company

Neuropace Inc

Inspection Date

March 5, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f7cd7549-8bd5-4eee-adab-3db41d2ea5f6

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