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FDA Inspection 834788 — Terumo Medical Corporation

Terumo Medical Corporation — FEI 1118880

The FDA completed an inspection of Terumo Medical Corporation on June 5, 2013 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
June 5, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Elkton, MD (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

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Recent compliance actions

FDA data resources