Establishment registration
LEJA PRODUCTS B.V.
FDA establishment registration 9614577 · NIEUW VENNEP Noord-Holland, NL
Key facts
| Registration number | 9614577 |
|---|---|
| Establishment name | LEJA PRODUCTS B.V. |
| Owner/operator | LEJA PRODUCTS B.V. |
| Owner/operator number | 9036023 |
| FEI number | 3002539673 |
| Address | LUZERNESTRAAT 10 |
| City | NIEUW VENNEP Noord-Holland |
| Country | NL |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | GHO |
| Device classes | 1 |
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