FDA Inspection 1333598 — Hitachi High Tech America, Inc. Radiation Therapy Division

Hitachi High Tech America, Inc. Radiation Therapy Division — FEI 3003993895

The FDA completed an inspection of Hitachi High Tech America, Inc. Radiation Therapy Division on Aug 7, 2026 in Santa Clara, CA. 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
Aug 7, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Clara, CA (United States)

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