FDA Inspection 1122411 — TERUMO YAMAGUCHI CORPORATION

TERUMO YAMAGUCHI CORPORATION — FEI 3013611763

The FDA completed an inspection of TERUMO YAMAGUCHI CORPORATION on Feb 19, 2020 in Yamaguchi. 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
Feb 19, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Yamaguchi (Japan)

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