FDA Inspection 1331290 — Nittobo Medical Company, Ltd., Medical Development Center

Nittobo Medical Company, Ltd., Medical Development Center — FEI 1000403749

The FDA completed an inspection of Nittobo Medical Company, Ltd., Medical Development Center on Jul 9, 2026 in Koriyama. 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
Jul 9, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Koriyama (Japan)

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