FDA Inspection 877631 — TERUMO CORPORATION

TERUMO CORPORATION — FEI 3003752255

The FDA completed an inspection of TERUMO CORPORATION on Apr 17, 2014 in Nakakoma-Gun. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Apr 17, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Nakakoma-Gun (Japan)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.