FDA Inspection 957132 - NeuroChaos Solutions Inc. - January 05, 2016

FDA Inspection 957132 for NeuroChaos Solutions Inc. on January 05, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 957132 for NeuroChaos Solutions Inc. on January 05, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

NeuroChaos Solutions Inc.

Inspection Date

January 5, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fde80716-31ad-4362-a01d-6a0faf978758

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