FDA Inspection 932660 - Philips North America, LLC - June 18, 2015

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Record Details

This FDA Inspection record concerns Philips North America, LLC, with an inspection on June 18, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Philips North America, LLC
Inspection Date: June 18, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 84508bf6-8949-4123-b675-3e2cbd018517

Violation Codes6

21 CFR 803.50(b)(1)21 CFR 820.100(a)21 CFR 820.30(f)21 CFR 820.30(g)21 CFR 820.5021 CFR 820.90(a)

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