FDA Device Establishments · JSON-LD · Markdown
FEI 1000391004 · Manufacture Medical Device · Status: Active
| FEI Number | 1000391004 |
|---|---|
| Owner / Operator | KEELER LTD. (#9011500) |
| Address | CLEWER HILL RD., WINDSOR, BERKSHIRE Windsor and Maidenhead, SL4 4AA, GB |
| Mandatory US Agent | Keeler USA |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HKY |
| Regulation § (21 CFR) | 886.1930 |
Source: openFDA. Public-domain (CC0).