FDA Inspection 936229 - Penumbra Inc. - August 04, 2015

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Record Details

This FDA Inspection record concerns Penumbra Inc., with an inspection on August 4, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Penumbra Inc.
Inspection Date: August 4, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 953eae88-8bf3-44dc-a358-663fdbf723dd