FDA Warning Letter — Philips North America, LLC

Case 63483 — FEI 1218950

The FDA took a Warning Letter action against Philips North America, LLC on October 9, 2009 (Andover, MA). 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
October 9, 2009
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Andover, MA (United States)