FDA Inspection 1166360 — CareFusion 303, Inc.

CareFusion 303, Inc. — FEI 2016493

The FDA completed an inspection of CareFusion 303, Inc. on Mar 10, 2022 in San Diego, CA. 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 10, 2022
Fiscal Year
2022
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.