Establishment registration
Guangzhou Aimooe Technology Co., Ltd.
FDA establishment registration 3032933985 · Guangzhou Guangdong, CN
Key facts
| Registration number | 3032933985 |
|---|---|
| Establishment name | Guangzhou Aimooe Technology Co., Ltd. |
| Owner/operator | Guangzhou Aimooe Technology Co., Ltd. |
| Owner/operator number | 10095882 |
| FEI number | 3032933985 |
| Address | Room 101, No.30-6 Kaitai Avenue, Huangpu District, 510700 Guangzhou, P.R.China |
| City | Guangzhou Guangdong |
| Country | CN |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | LPP |
| Device classes | 2 |
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