FDA Device Establishments · JSON-LD · Markdown
FEI 3010508078 · Complaint File Establishment per 21 CFR 820.198 Export Device to the United States But Perform No Other Operation on Device Manufacture Medical Device · Status: Active
| FEI Number | 3010508078 |
|---|---|
| Owner / Operator | Keter Canada, Inc. (#10045078) |
| Address | 205 Market Drive, Milton Ontario, L9T 4Z7, CA |
| Mandatory US Agent | Registrar Corp |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MMK |
| Regulation § (21 CFR) | 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. Public-domain (CC0).