FDA Inspection 1026939 - Bunnell, Inc. - August 08, 2017

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Record Details

This FDA Inspection record concerns Bunnell, Inc., with an inspection on August 8, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Bunnell, Inc.
Inspection Date: August 8, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 94800c4f-56d8-4f52-90e4-370c4193d241