FDA Device Establishments · JSON-LD · Markdown
FEI 3001239013 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3001239013 |
|---|---|
| Owner / Operator | Angelini Pharma Inc. (#10027838) |
| Address | 230 Peachtree Street NW, Suite 1250, ATL, GA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | KDJ |
| Regulation § (21 CFR) | 876.5630 |
| Proprietary names | Alcavis 50 |
Source: openFDA. Public-domain (CC0).