FDA Inspection 1031329 — Abbott Vascular Inc

Abbott Vascular Inc — FEI 2024168

The FDA completed an inspection of Abbott Vascular Inc on Oct 4, 2017 in Temecula, 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
Oct 4, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Temecula, CA (United States)

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