Establishment registration
ZHEJIANG ANJI HUABU INDUSTRIAL CO., LTD.
FDA establishment registration 9710020 · HUZHOU Zhejiang, CN
Key facts
| Registration number | 9710020 |
|---|---|
| Establishment name | ZHEJIANG ANJI HUABU INDUSTRIAL CO., LTD. |
| Owner/operator | Zhejiang Anji Huabu Industrial Co., Ltd. |
| Owner/operator number | 9045080 |
| FEI number | 3003340795 |
| Address | Building 1-2, No. 588 Dragon King Creek Middle Road, Dipu Street |
| City | HUZHOU Zhejiang |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | BSY, BYZ, CAT, CCQ, EXG, EYI, FAQ, FGY, FMA, FOD, FPF, FQM, FXO, GEC, HED, ILG, ILH, IPM, ITG, JCY, JYH, KCJ, KGX, KIC, KXF, KYZ, LGF, LRJ, LYU, NAD and 2 more |
| Device classes | 1, 2 |
At a glance
- 10–99 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