CareFusion 213, LLC
FDA regulatory history for CareFusion 213, LLC: 18 Form 483s, 1 Warning Letter, 37 Recalls.
18Form 483s
1Warning Letters
37Recalls
56Total Actions
Jul 09, 2026Last Event
Total Actions = Form 483s + Warning Letters + Recalls.
Facility types: Pharmaceutical
See the regulatory timeline, risk score, GMP issue radar, peer comparison, and document downloads on the 483 Signal dashboard.
This profile aggregates publicly available FDA documents and does not constitute an assessment of this company's compliance status. Companies may have taken corrective actions not yet reflected in public records. Provided for informational purposes only.