FDA Inspection 869798 — Abbott Vascular

Abbott Vascular — FEI 3005718570

The FDA completed an inspection of Abbott Vascular on March 14, 2014 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
March 14, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Clonmel (Ireland)

Additional Details

Postmarket Audit Inspections