# Keter Canada Inc.

FEI: 3010508078
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device
Owner/operator: Keter Canada, Inc. (#10045078)

Address: 205 Market Drive, Milton Ontario, L9T 4Z7, CA

Mandatory US Agent: Registrar Corp

## Products

Total registered: 1
Top product codes: MMK
Regulation §: 880.5570

Proprietary names: AP Medical, AP 60 DUO (18 Gal DUO lid), AP 30 DUO (8 Gal DUO lid), AP 60 MONO (18 Gal MONO lid), AP 50 MONO (12 Gal MONO lid), AP 50 DUO (12 Gal DUO lid), AP 30 MONO (8 Gal MONO lid), AP 5.4 QT, PBS 12 Lt

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010508078%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010508078