FDA Device Establishments · JSON-LD · Markdown
FEI 3015738702 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3015738702 |
|---|---|
| Owner / Operator | Omnitech Labs Inc. (#10089962) |
| Address | 215 Seminaire Blvd South Suite 1305, St-Jean-sur-Richelieu Quebec, J3B 8W1, CA |
| Mandatory US Agent | Registrar Corp |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | JQP |
| Regulation § (21 CFR) | 862.2100 |
| Proprietary names | OMNI-Lab |
Source: openFDA. Public-domain (CC0).