FDA Device Establishments · JSON-LD · Markdown
FEI 3014083954 · Foreign Private Label Distributor Complaint File Establishment per 21 CFR 820.198 Export Device to the United States But Perform No Other Operation on Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3014083954 |
|---|---|
| Owner / Operator | ActivInsights Ltd. (#10056642) |
| Address | 6 Nene Road, Bicton Industrial Park, Kimbolton Cambridgeshire, PE28 0LF, GB |
| Mandatory US Agent | GBM Authorized Representative Ltd. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | IKK |
| Regulation § (21 CFR) | 890.1925 |
| Proprietary names | GENEActiv |
Source: openFDA. Public-domain (CC0).