FDA Device Establishments · JSON-LD · Markdown
FEI 3003917514 · Foreign Private Label Distributor Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3003917514 |
|---|---|
| Owner / Operator | BTNX Inc. (#9058575) |
| Address | 722 Rosebank Road, Pickering Ontario, L1W 4B2, CA |
| Mandatory US Agent | Phil Triolo and Associates LC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 11 |
| Product codes (top 20) | QAW, NGL, QBF, NGG, NFY, NFT, PTH, PTG, NFV, LCM, NFW |
| Regulation § (21 CFR) | 862.3910, 862.3650, 862.3700, 862.3610, 862.3250, 862.3100, 862.3150, 862.3620, 862.3170, 862.3870 |
| Proprietary names | Rapid Response Home Drug Monitoring Panel; Rapid Response Drug Monitoring Panel |
Source: openFDA. Public-domain (CC0).