# OMNITECH LABS INC.

FEI: 3015738702
Status: Active
Establishment types: Manufacture Medical Device; Complaint File Establishment per 21 CFR 820.198
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

## Products

Total registered: 1
Top product codes: JQP
Regulation §: 862.2100

Proprietary names: OMNI-Lab

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223015738702%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3015738702