Establishment registration
Goertek Inc
FDA establishment registration 3046005946 · Weifang Shandong, CN
Key facts
| Registration number | 3046005946 |
|---|---|
| Establishment name | Goertek Inc |
| Owner/operator | Goertek Inc |
| Owner/operator number | 10052631 |
| FEI number | 3046005946 |
| Address | No.999, Liyuan Street, Hi-Tech Industrial Development District, |
| City | Weifang Shandong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | HQY, HQZ |
| 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