FDA Inspection 1023742 - Philips Electronics North America Corporation - August 31, 2017

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Record Details

This FDA Inspection record concerns Philips Electronics North America Corporation, with an inspection on August 31, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Philips Electronics North America Corporation
Inspection Date: August 31, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · d19a8b7e-1f44-4797-be5d-23749eb13383