FDA Device Establishments · JSON-LD · Markdown
FEI 1281412 · Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 1281412 |
|---|---|
| Owner / Operator | Centrix, Inc. (#1281412) |
| Address | 770 River Rd, Shelton, CT, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 2 |
| Product codes (top 20) | MVL, ELW |
| Regulation § (21 CFR) | 872.3660 |
Source: openFDA. Public-domain (CC0).