FDA Warning Letter — Philips North America LLC

Case 142931 — FEI 1000524572

The FDA took a Warning Letter action against Philips North America LLC on Mar 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
Mar 28, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Bothell, WA (United States)

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