FDA Inspection 1073302 - Philips North America LLC - December 03, 2018

FDA Inspection 1073302 for Philips North America LLC on December 03, 2018. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 1073302 for Philips North America LLC on December 03, 2018. Classification: Official Action Indicated (OAI).

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Record Information

Company

Philips North America LLC

Inspection Date

December 3, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd06173c-a691-4681-bd6d-ce4d541fb130

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