FDA inspection
GUIDEMIA TECHNOLOGIES LLC: FDA inspection ending Jul 6, 2026
FDA inspection 1325530 · Voluntary Action Indicated (VAI) · Buena Park, CA
Key facts
| Inspection ID | 1325530 |
|---|---|
| Firm | GUIDEMIA TECHNOLOGIES LLC |
| FEI number | 3013634985 |
| City | Buena Park |
| State | CA |
| ZIP | 90620 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Jul 6, 2026 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes 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