FDA Device Establishments · JSON-LD · Markdown
FEI 3014150042 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3014150042 |
|---|---|
| Owner / Operator | TightLine Development (#10056000) |
| Address | One Glenlake Parkway, Suite 650, Atlanta, GA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KDD |
| Regulation § (21 CFR) | 878.4800 |
| Proprietary names | eXodus |
Source: openFDA. Public-domain (CC0).