Philips North America LLC

Form 483

Bothell, Washington, United StatesFEI 1000524572Issued March 19, 2012

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.

Observations1

Issue DateMarch 19, 2012

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Philips North America LLC
Location: Bothell, Washington, United States
FEI Number: 1000524572
Product Type: Devices
Issue Date: March 19, 2012
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.

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Philips North America LLC FDA Form 483, Bothell, Washington, March 19, 2012