FDA Device Establishments · JSON-LD · Markdown
FEI 3017199812 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3017199812 |
|---|---|
| Owner / Operator | GPI USA, Inc. (#10076947) |
| Address | 2200 Post Oak Blvd, Suite 1000, Houston, TX, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MMH |
| Regulation § (21 CFR) | 864.9165 |
| Proprietary names | ElDorado Donor 4 |
Source: openFDA. Public-domain (CC0).