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FDA Inspection
•Penumbra Inc.•February 23, 2016

FDA Inspection 965001 - Penumbra Inc. - February 23, 2016

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Record Details

This FDA Inspection record concerns Penumbra Inc., with an inspection on February 23, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Penumbra Inc.
Inspection Date
February 23, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
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ID · 1ab9bdfb-6166-4734-8c79-6db7a2a37be1

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