Establishment registration
CITOTEST SCIENTIFIC CO.,LTD.
FDA establishment registration 3015505238 · Nanjing Jiangsu, CN
Key facts
| Registration number | 3015505238 |
|---|---|
| Establishment name | CITOTEST SCIENTIFIC CO.,LTD. |
| Owner/operator | Citotest Scientific Co.,Ltd. |
| Owner/operator number | 10061360 |
| FEI number | 3015505238 |
| Address | 8th,Floor,Building 7,89 Shengli Road,Jiangning District |
| City | Nanjing Jiangsu |
| Country | CN |
| Establishment types | Foreign exporter |
| Registration valid through | 2026 |
| Product codes listed | FMA, FMH, FNY, GHC, GHK, GJW, HYB, HYK, HYL, IBJ, IBK, IBL, IDR, IDS, IDW, IDZ, JQC, JRB, JRC, JRL, JRO, JRQ, JSG, JSM, KDT, KEO, KER, KES, KET, KEW and 16 more |
| Device classes | 1 |
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