FDA Warning Letter — CareFusion 303, Inc.

Case 691601 — FEI 2016493

The FDA took a Warning Letter action against CareFusion 303, Inc. on November 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
November 22, 2024
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
San Diego, CA (United States)