FDA Device Establishments · JSON-LD · Markdown
FEI 3030927217 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3030927217 |
|---|---|
| Owner / Operator | HOLOGIC, INC. (#9007676) |
| Address | Kaiserin-Augusta-Allee 112/113, Berlin, 10553, DE |
| Mandatory US Agent | MEDAGENT Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | NEU |
| Regulation § (21 CFR) | 878.4300 |
| Proprietary names | Tumark Professional Q |
Source: openFDA. Public-domain (CC0).