Establishment registration
OMNITECH LABS INC.
FDA establishment registration 3015738702 · St-Jean-sur-Richelieu Quebec, CA
Key facts
| Registration number | 3015738702 |
|---|---|
| Establishment name | OMNITECH LABS INC. |
| Owner/operator | Omnitech Labs Inc. |
| Owner/operator number | 10089962 |
| FEI number | 3015738702 |
| Address | 215 Seminaire Blvd South Suite 1305 |
| City | St-Jean-sur-Richelieu Quebec |
| Country | CA |
| Establishment types | Manufacturer, Complaint file establishment |
| Registration valid through | 2026 |
| Product codes listed | JQP |
| Device classes | 1 |
At a glance
- 1–9 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