FDA Device Establishments · JSON-LD · Markdown
FEI 1815703 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 1815703 |
|---|---|
| Owner / Operator | LIQUIPAK CORP. (#1815703) |
| Address | 2205 REDMAN DRIVE, Alma, MI, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | LRJ |
| Regulation § (21 CFR) | 880.6890 |
| Proprietary names | Vesta-Syde Decontamination System |
Source: openFDA. Public-domain (CC0).