FDA Inspection 937627 — Abbott Vascular

Abbott Vascular — FEI 3005718570

The FDA completed an inspection of Abbott Vascular on Jul 23, 2015 in Clonmel. 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
Jul 23, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Clonmel (Ireland)

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