FDA Inspection 1031113 — Abbott Vascular

Abbott Vascular — FEI 3006604866

The FDA completed an inspection of Abbott Vascular on Oct 10, 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 10, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Temecula, CA (United States)

Additional Details

Postmarket Audit Inspections

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