FDA Inspection 891123 - VIVEVE DENVER - August 01, 2014

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Record Details

This FDA Inspection record concerns VIVEVE DENVER, with an inspection on August 1, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: VIVEVE DENVER
Inspection Date: August 1, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · bf8c6433-0d91-4e39-b9aa-5217bdce991e