FDA Inspection 872272 - Coagusense, Inc. - March 31, 2014

FDA Inspection 872272 for Coagusense, Inc. on March 31, 2014. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 872272 for Coagusense, Inc. on March 31, 2014. Classification: No Action Indicated (NAI).

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Record Information

Company

Coagusense, Inc.

Inspection Date

March 31, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc26169c-f106-4064-b320-65356f2d38c7

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