Establishment registration
ARMIS BIOPHARMA, INC.
FDA establishment registration 3020745223 · Fort Collins, US
Key facts
| Registration number | 3020745223 |
|---|---|
| Establishment name | ARMIS BIOPHARMA, INC. |
| Owner/operator | Armis Biopharma, Inc. |
| Owner/operator number | 10083045 |
| FEI number | 3020745223 |
| Address | 2401 Research Blvd Ste 205 |
| City | Fort Collins |
| State | CO |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | FQH, FRO, HTY |
| Device classes | 2, U |
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