FDA Warning Letter — Philips North America LLC

Case 142931 — FEI 1000524572

The FDA took a Warning Letter action against Philips North America LLC on March 28, 2011 (Bothell, WA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Philips North America LLC
Date
March 28, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Bothell, WA (United States)