FDA Device Establishments · JSON-LD · Markdown
FEI 1050190 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 1050190 |
|---|---|
| Owner / Operator | U.S. GOVERNMENT DEPARTMENT HHS (#1050190) |
| Address | 1600 CLIFTON RD., N.E., ATLANTA, GA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | PBK |
| Regulation § (21 CFR) | 866.3315 |
| Proprietary names | Non-variola Orthopoxvirus Real-time PCR Primer and Probe Set |
Source: openFDA. Public-domain (CC0).