FDA Inspection 999616 — Abbott Vascular

Abbott Vascular — FEI 3005718570

The FDA completed an inspection of Abbott Vascular on December 9, 2016 in Clonmel. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 9, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Clonmel (Ireland)

Additional Details

Postmarket Audit Inspections