Establishment registration
Abbott Rapid Dx North America, LLC
FDA establishment registration 3006984151 · Lake Mary, US
Key facts
| Registration number | 3006984151 |
|---|---|
| Establishment name | Abbott Rapid Dx North America, LLC |
| Owner/operator | ABBOTT LABORATORIES |
| Owner/operator number | 1415939 |
| FEI number | 3006984151 |
| Address | 1101 Greenwood Blvd Unit 4001 |
| City | Lake Mary |
| State | FL |
| Country | US |
| Registration valid through | 2026 |
At a glance
- 1–9 Device listings
- None 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