FDA Inspection 893045 — CareFusion 303, Inc.

CareFusion 303, Inc. — FEI 2016493

The FDA completed an inspection of CareFusion 303, Inc. on Sep 29, 2014 in San Diego, CA. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Sep 29, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

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