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Philips North America LLC — FDA Facility Profile

FEI 1218950

Philips North America LLC is an FDA-registered facility (FEI 1218950) located in ANDOVER, MA, US. RegDataLab tracks 6 FDA inspections and 1 compliance action at this facility.

Facility Details

Location
ANDOVER, MA (US)
Registration Expires
N/A
Operations
Source
device

Recent inspections

  • 1073570 (OAI Tue Dec 04 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 932660 (OAI Thu Jun 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 860079 (OAI Thu Dec 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 747102 (NAI Wed Sep 28 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 701792 (NAI Tue Dec 14 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 569821 (OAI Tue Mar 10 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Import refusals

  • 799-3973714-5/11/1 (Fri Oct 25 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-6517302-1/51/1 (Thu Dec 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-5135593-7/1/1 (Fri Apr 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • UPS-2531056-6/1/1 (Thu Sep 17 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • D51-1130290-2/1/1 (Tue Mar 04 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • D51-1129944-7/1/1 (Wed Jan 08 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • D51-1129944-7/2/1 (Wed Jan 08 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • D51-1129944-7/3/1 (Wed Jan 08 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-1542614-6/1/1 (Thu Dec 19 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-1135606-6/1/1 (Thu Aug 08 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources