FDA Inspection 997744 — CareFusion 213, LLC
The FDA completed an inspection of CareFusion 213, LLC on Dec 15, 2016 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
- Dec 15, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- El Paso, TX (United States)