FDA Device Establishments · JSON-LD · Markdown
FEI 1000122536 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 1000122536 |
|---|---|
| Owner / Operator | QuidelOrtho Corporation (#2024674) |
| Address | 2005 East State Street, Suite 100, ATHENS, OH, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GNW |
| Regulation § (21 CFR) | 866.3330 |
| Proprietary names | D3 Ultra DFA Respiratory Virus Scre |
Source: openFDA. Public-domain (CC0).