FDA Device Establishments · JSON-LD · Markdown
FEI 3010388769 · Repack or Relabel Medical Device Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3010388769 |
|---|---|
| Owner / Operator | The Morel Company (#10044676) |
| Address | 300 Winding Way, Batesville, IN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FMR |
| Regulation § (21 CFR) | 880.6785 |
| Proprietary names | Hercules Sheet |
Source: openFDA. Public-domain (CC0).