FDA Inspection 999616 — Abbott Vascular

Abbott Vascular — FEI 3005718570

The FDA completed an inspection of Abbott Vascular on Dec 9, 2016 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
Dec 9, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Clonmel (Ireland)

Additional Details

Postmarket Audit Inspections

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