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FDA Inspection 997744 — CareFusion 213, LLC

CareFusion 213, LLC — FEI 3004932373

The FDA completed an inspection of CareFusion 213, LLC on December 15, 2016 in El Paso, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 15, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
El Paso, TX (United States)

Facility

Other inspections at this facility

  • 1288506 (OAI Fri Oct 24 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1219336 (VAI Fri Sep 29 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 871049 (NAI Tue Mar 11 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 818062 (VAI Fri Feb 08 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 729730 (OAI Fri Jun 03 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources