Establishment registration
HI-P (XIAMEN) PRECISION PLASTIC MANUFACTURING CO.,
FDA establishment registration 3005607635 · XIAMEN Fujian, CN
Key facts
| Registration number | 3005607635 |
|---|---|
| Establishment name | HI-P (XIAMEN) PRECISION PLASTIC MANUFACTURING CO., |
| Owner/operator | HI-P (XIAMEN) PRECISION PLASTIC MANUFACTURING CO., |
| Owner/operator number | 9083459 |
| FEI number | 3005607635 |
| Address | No. 5, Haijing Dongsan Road, Bonded Port Area Xiamen Area of Polit Free Trade Zone |
| City | XIAMEN Fujian |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | EEG, EFS, EFW, JEQ, JES, KYX |
| 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