FDA Inspection 1035423 - TherOx, Inc. - November 29, 2017

FDA Inspection 1035423 for TherOx, Inc. on November 29, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1035423 for TherOx, Inc. on November 29, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

TherOx, Inc.

Inspection Date

November 29, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa2a7a49-fdd2-4f7e-a070-cae8154142fb

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