FDA Inspection 992622 - Verathon, Inc. - November 03, 2016

FDA Inspection 992622 for Verathon, Inc. on November 03, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 992622 for Verathon, Inc. on November 03, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Verathon, Inc.

Inspection Date

November 3, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f7f17b90-2c7e-4d89-ba40-144a83487d2d

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