FDA Inspection 871049 — CareFusion 213, LLC

CareFusion 213, LLC — FEI 3004932373

The FDA completed an inspection of CareFusion 213, LLC on Mar 11, 2014 in El Paso, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 11, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
El Paso, TX (United States)

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