Home / Compliance actions / 265

FDA Injunction — Philips North America LLC

Case 265 — FEI 1000524572

The FDA took a Injunction action against Philips North America LLC on Oct 31, 2017 (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
Oct 31, 2017
Fiscal Year
2018
Product Type
Devices
Center
CDRH
Location
Bothell, WA (United States)

Facility

Recent inspections

Other compliance actions

FDA data resources

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