FDA Device Establishments · JSON-LD · Markdown
FEI 3014022295 · Manufacture Device in the United States for Export Only · Status: Active
| FEI Number | 3014022295 |
|---|---|
| Owner / Operator | PHASE Diagnostics (#10075679) |
| Address | 10527 Garden Grove Blvd., Garden Grove, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | QKO |
| Proprietary names | INDICAID COVID-19 IgM/IgG Rapid Test |
Source: openFDA. Public-domain (CC0).