Establishment registration
KINGSWAY PHARMACEUTICALS DBA NFI, LLC
FDA establishment registration 3013167221 · Bristol, US
Key facts
| Registration number | 3013167221 |
|---|---|
| Establishment name | KINGSWAY PHARMACEUTICALS DBA NFI, LLC |
| Owner/operator | Kingsway Pharmaceuticals dba NFI, LLC |
| Owner/operator number | 10053911 |
| FEI number | 3013167221 |
| Address | 636 Shelby Street |
| City | Bristol |
| State | TN |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | JMT, LCX, LJX, NAC, NGA, NGE |
| Device classes | 1, 2 |
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