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FDA Inspection 555781 — Philips North America LLC

Philips North America LLC — FEI 1000524572

The FDA completed an inspection of Philips North America LLC on December 16, 2008 in Bothell, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 16, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Bothell, WA (United States)

Facility

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Recent compliance actions

FDA data resources