FDA Device Establishments · JSON-LD · Markdown
FEI 3023296261 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3023296261 |
|---|---|
| Owner / Operator | Citest Diagnostics Inc. (#10090628) |
| Address | 170-422, RICHARDS ST, VANCOUVER British Columbia, V6B 2Z4, CA |
| Mandatory US Agent | ACESO LABORATORIES INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 23 |
| Product codes (top 20) | LDJ, LCM, NFW, NGL, NFY, JXM, NGM, LAF, DJG, PTG, LFG, DKZ, NFV, DIS, NFT, DIO, NGG, DNK, DJC, DJR |
| Regulation § (21 CFR) | 862.3870, 862.3650, 862.3250, 862.3170, 862.3610, 862.3620, 862.3910, 862.3100, 862.3150, 862.3640 |
| Proprietary names | Citest Multiplex DOA Home Test Cup (Urine); Citest Multiplex DOA Home Test Panel (Urine); Citest Multiplex DOA Test Panel (Urine); Citest Multiplex DOA Test Cup (Urine) |
Source: openFDA. Public-domain (CC0).