Establishment registration
ALTA DIAGNOSTICS, INC.
FDA establishment registration 2084170 · Carson City, US
Key facts
| Registration number | 2084170 |
|---|---|
| Establishment name | ALTA DIAGNOSTICS, INC. |
| Owner/operator | ALTA DIAGNOSTICS, INC. |
| Owner/operator number | 9000337 |
| FEI number | 2084170 |
| Address | 3123 Research Way Ste 214 |
| City | Carson City |
| State | NV |
| Country | US |
| Establishment types | Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | JJW |
| Device classes | 1 |
At a glance
- 1–9 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- None 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