FDA Device Establishments · JSON-LD · Markdown
FEI 3007606081 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3007606081 |
|---|---|
| Owner / Operator | Wondfo USA Co., Ltd. (#10028951) |
| Address | 890 Remington Blvd, Bolingbrook, IL, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 8 |
| Product codes (top 20) | DKZ, LDJ, JXM, DJG, DIO, LAF, LCM, DIS |
| Regulation § (21 CFR) | 862.3100, 862.3870, 862.3170, 862.3650, 862.3250, 862.3610, 862.3150 |
| Proprietary names | Easy@Home Multi-Drug Urine Test Cup; Easy@Home Multi-Drug Urine Test Panel; Multi-Drug Urine Test Cup, Multi-Drug Urine Test Panel |
Source: openFDA. Public-domain (CC0).