FDA Inspection 1005211 - Philips North America - March 03, 2017

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Record Details

This FDA Inspection record concerns Philips North America, with an inspection on March 3, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Philips North America
Inspection Date: March 3, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · e2cb00cf-409d-4f2c-b923-99f98a7a6b0a

Violation Codes1

21 CFR 820.184

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