FDA Warning Letter — Philips North America, LLC

Case 63483 — FEI 1218950

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.