FDA Inspection 830352 - Philips North America LLC - April 24, 2013

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Record Details

This FDA Inspection record concerns Philips North America LLC, with an inspection on April 24, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Philips North America LLC
Inspection Date: April 24, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 12821d9a-7ffe-4fb6-a6c4-abbabf9472a4

Violation Codes5

21 CFR 820.100(a)21 CFR 820.5021 CFR 820.50(a)(1)21 CFR 820.50(a)(3)21 CFR 820.80(a)

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