FDA Warning Letter — CareFusion 303, Inc.

Case 691601 — FEI 2016493

The FDA took a Warning Letter action against CareFusion 303, Inc. on Nov 22, 2024 (San Diego, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
CareFusion 303, Inc.
Date
Nov 22, 2024
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
San Diego, CA (United States)

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