FDA Inspection 569821 - Philips North America, LLC - March 10, 2009

Record Details

This FDA Inspection record concerns Philips North America, LLC, with an inspection on March 10, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Philips North America, LLC
Inspection Date: March 10, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · de9ee8ca-f41d-432c-bb13-46b2d7ab66e6

Violation Codes7

21 CFR 803.50(a)(1)21 CFR 803.50(a)(2)21 CFR 806.10(b)21 CFR 820.100(a)(3)21 CFR 820.150(a)21 CFR 820.184(d)21 CFR 820.198(a)(1)

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