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FDA Inspection 1310026 — Avantec Vascular Corporation

Avantec Vascular Corporation — FEI 3003524171

The FDA completed an inspection of Avantec Vascular Corporation on March 24, 2026 in Sunnyvale, 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
March 24, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sunnyvale, CA (United States)

Facility

Other inspections at this facility

  • 1195638 (VAI Thu Jan 26 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1114776 (VAI Fri Jan 10 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 833402 (NAI Tue May 14 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 667195 (NAI Thu Jun 17 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources