FDA Device Establishments · JSON-LD · Markdown
FEI 1017835 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 1017835 |
|---|---|
| Owner / Operator | BECKMAN COULTER, INC. (#2050012) |
| Address | 740 WEST 83RD ST., HIALEAH, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | JPK |
| Regulation § (21 CFR) | 864.8625 |
| Proprietary names | Retic-X Cell Control |
Source: openFDA. Public-domain (CC0).