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FDA Inspection 1031329 — Abbott Vascular Inc

Abbott Vascular Inc — FEI 2024168

The FDA completed an inspection of Abbott Vascular Inc on October 4, 2017 in Temecula, CA. 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
October 4, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Temecula, CA (United States)

Facility

Other inspections at this facility

  • 1223681 (NAI Fri Oct 27 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1179404 (NAI Tue Aug 23 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1157715 (NAI Wed Nov 03 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 987224 (NAI Fri Apr 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 906402 (NAI Mon Nov 24 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources