FDA Device Establishments · JSON-LD · Markdown
FEI 3012447313 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3012447313 |
|---|---|
| Owner / Operator | Viospex (#10051911) |
| Address | 7647 E. Windlawn Way, Parker, CO, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HDL |
| Regulation § (21 CFR) | 884.4520 |
| Proprietary names | The Bouquet Speculum |
Source: openFDA. Public-domain (CC0).