FDA Inspection 1073224 — Ashitaka Factory Of Terumo Corporation

Ashitaka Factory Of Terumo Corporation — FEI 3002808327

The FDA completed an inspection of Ashitaka Factory Of Terumo Corporation on Oct 31, 2018 in Fujinomiya. 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
Oct 31, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Fujinomiya (Japan)