FDA Inspection 950339 - Nexus CMF, LLC - October 01, 2015

FDA Inspection 950339 for Nexus CMF, LLC on October 01, 2015. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 950339 for Nexus CMF, LLC on October 01, 2015. Classification: No Action Indicated (NAI).

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Record Information

Company

Nexus CMF, LLC

Inspection Date

October 1, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f9bd283f-cf7c-4fc0-a48b-fc4b654d9c75

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