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FDA Inspection 1182280 — Terumo Medical Corporation

Terumo Medical Corporation — FEI 1118880

The FDA completed an inspection of Terumo Medical Corporation on October 28, 2022 in Elkton, MD. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 28, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Elkton, MD (United States)

Facility

Other inspections at this facility

  • 1317212 (NAI Fri May 01 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1094113 (VAI Thu Jun 20 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1003680 (NAI Fri Jan 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 950051 (OAI Fri Oct 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 847650 (VAI Thu Sep 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources