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FDA Inspection 996655 — Terumo Cardiovascular Systems Corporation

Terumo Cardiovascular Systems Corporation — FEI 1828100

The FDA completed an inspection of Terumo Cardiovascular Systems Corporation on December 7, 2016 in Ann Arbor, MI. 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
December 7, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Ann Arbor, MI (United States)

Facility

Other inspections at this facility

  • 1147794 (NAI Wed Jul 14 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1111814 (NAI Fri Oct 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1031879 (NAI Tue Oct 03 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 971672 (NAI Fri May 13 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 912380 (NAI Fri Jan 30 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

  • Injunction (138) (Tue Mar 29 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources