FDA Inspection 1002192 - Penumbra Inc. - February 13, 2017

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Record Details

This FDA Inspection record concerns Penumbra Inc., with an inspection on February 13, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Penumbra Inc.
Inspection Date: February 13, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1db6d982-aa3a-46c1-ac89-e28f3137708b