FDA Inspection 1278127 — CareFusion DR 203 LTD

CareFusion DR 203 LTD — FEI 3007019930

The FDA completed an inspection of CareFusion DR 203 LTD on September 18, 2025 in Santo Domingo. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 18, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Santo Domingo (Dominican Republic (the))