FDA inspection
Hitachi High Tech America, Inc. Radiation Therapy Division: FDA inspection ending Aug 7, 2026
FDA inspection 1333598 · No Action Indicated (NAI) · Santa Clara, CA
Key facts
| Inspection ID | 1333598 |
|---|---|
| Firm | Hitachi High Tech America, Inc. Radiation Therapy Division |
| FEI number | 3003993895 |
| City | Santa Clara |
| State | CA |
| ZIP | 95054 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Aug 7, 2026 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data