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FDA Inspection 1317212 — Terumo Medical Corporation

Terumo Medical Corporation — FEI 1118880

The FDA completed an inspection of Terumo Medical Corporation on May 1, 2026 in Elkton, MD. 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
May 1, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Elkton, MD (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

Other inspections at this facility

  • 1182280 (NAI Fri Oct 28 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1094113 (VAI Thu Jun 20 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1003680 (VAI 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