Establishment registration
CAROLON CO.
FDA establishment registration 1043551 · RURAL HALL, US
Key facts
| Registration number | 1043551 |
|---|---|
| Establishment name | CAROLON CO. |
| Owner/operator | CAROLON CO. |
| Owner/operator number | 1043551 |
| FEI number | 1043551 |
| Address | 601 FORUM PKWY. |
| City | RURAL HALL |
| State | NC |
| Country | US |
| Establishment types | Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | DWL, FQL, FQM, ILG, IMA, KYR |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- None 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