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FDA Inspection 1073570 — Philips North America, LLC

Philips North America, LLC — FEI 1218950

The FDA completed an inspection of Philips North America, LLC on December 4, 2018 in Andover, MA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
December 4, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Andover, MA (United States)

Facility

Other inspections at this facility

  • 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))

Recent compliance actions

FDA data resources