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NIPRO VASCULAR CORPORATION — FDA Facility Profile

FEI 3007835716

NIPRO VASCULAR CORPORATION is an FDA-registered facility (FEI 3007835716) located in Nagoya Aichi, JP. RegDataLab tracks 2 FDA inspections at this facility.

Facility Details

Location
Nagoya Aichi (JP)
Registration Expires
N/A
Operations
Source
device

Recent inspections

  • 1269122 (NAI Thu Apr 03 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1227869 (VAI Thu Jan 25 2024 00:00:00 GMT+0000 (Coordinated Universal Time))

Import refusals

  • FR1-0019245-4/10002/2 (Tue Aug 19 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0019245-4/10002/1 (Tue Aug 19 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0019201-7/11/1 (Thu May 08 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0019201-7/31/1 (Thu May 08 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0018965-8/21/1 (Thu Mar 06 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0018965-8/11/1 (Thu Mar 06 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0018687-8/21/1 (Tue Feb 25 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0018687-8/11/1 (Tue Feb 25 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0019071-4/11/1 (Tue Dec 03 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • FR1-0019071-4/21/1 (Tue Dec 03 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources