FDA Inspection 877631 — TERUMO CORPORATION

TERUMO CORPORATION — FEI 3003752255

The FDA completed an inspection of TERUMO CORPORATION on April 17, 2014 in Nakakoma-Gun. 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
April 17, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Nakakoma-Gun (Japan)