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FDA Inspection 950051 — Terumo Medical Corporation

Terumo Medical Corporation — FEI 1118880

The FDA completed an inspection of Terumo Medical Corporation on October 23, 2015 in Elkton, MD. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
October 23, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Elkton, MD (United States)

Facility

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Recent compliance actions

FDA data resources