Philips North America, LLC

Form 483

Andover, Massachusetts, United StatesFEI 1218950Issued December 12, 2013

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.

Observations12

Issue DateDecember 12, 2013

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: December 12, 2013
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, December 12, 2013