Establishment registration
APIXIA INC.
FDA establishment registration 3008361230 · City of Industry, US
Key facts
| Registration number | 3008361230 |
|---|---|
| Establishment name | APIXIA INC. |
| Owner/operator | APIXIA INC. |
| Owner/operator number | 10031841 |
| FEI number | 3008361230 |
| Address | 18688 E. SAN JOSE AVE |
| City | City of Industry |
| State | CA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | EGZ, EHA, EHD, IWZ, KQM, MUH, NRD |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- 1–9 FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database