Philips North America, LLC

Form 483

Andover, Massachusetts, United StatesFEI 1218950Issued June 18, 2015

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 1218950.

Observations6

Issue DateJune 18, 2015

StatusNo Warning Letter

Related Inspections6

Establishment Details

Firm: Philips North America, LLC
Location: Andover, Massachusetts, United States
FEI Number: 1218950
Product Type: Devices
Issue Date: June 18, 2015
Country: United States

Inspection History, 2009 to 2018

NAI1

VAI1

OAI4

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, Andover, Massachusetts, June 18, 2015