FDA Device Establishments · JSON-LD · Markdown
FEI 1038758 · Repack or Relabel Medical Device Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 1038758 |
|---|---|
| Owner / Operator | ASO LLC (#1038758) |
| Address | 300 SARASOTA CENTER BLVD., SARASOTA, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | GEH |
| Regulation § (21 CFR) | 878.4350 |
Source: openFDA. Public-domain (CC0).