Establishment registration
Li Wai Precision International Limited
FDA establishment registration 3009582259 · Tsimshatsui, Kowloon, HK
Key facts
| Registration number | 3009582259 |
|---|---|
| Establishment name | Li Wai Precision International Limited |
| Owner/operator | Guangzhou Aquila Precise Tools Limited |
| Owner/operator number | 10044682 |
| FEI number | 3009582259 |
| Address | RM 1804, 18/F, Cheuk Nang Centre, No. 9 Hillwood Road, |
| City | Tsimshatsui, Kowloon |
| Country | HK |
| Establishment types | Manufacturer, Contract manufacturer |
| Registration valid through | 2026 |
| Product codes listed | FSM, FXZ, FZX, GFA, GFC, GFG, HRT, HTD, HTO, HTQ, HTR, HTW, HTZ, HWA, HWB, HWE, HWR, HWT, HWX, HXX, JWH, KTZ, LPH, LRY, LXH, LYS, MBH, QBO |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 1,000+ 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