FDA Inspection 860079 - Philips North America, LLC - December 12, 2013

FDA Inspection 860079 for Philips North America, LLC on December 12, 2013. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 860079 for Philips North America, LLC on December 12, 2013. Classification: No Action Indicated (NAI).

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Record Information

Company

Philips North America, LLC

Inspection Date

December 12, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f74e4d68-9a73-4ef7-803d-9de447191c98

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