Philips North America LLC

Form 483FOIA Uncovered

Bothell, WashingtonFEI 1000524572Issued December 03, 2018

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1000524572.

ObservationsNot available

Issue DateDecember 03, 2018

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Philips North America LLC
Location: Bothell, Washington
FEI Number: 1000524572
Product Type: Devices
Issue Date: December 03, 2018
Country: United States

Inspection History, 2008 to 2022

NAI1

VAI6

OAI3

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

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Philips North America LLC FDA Form 483, Bothell, Washington, December 3, 2018