FDA Device Establishments · JSON-LD · Markdown
FEI 1000123463 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 1000123463 |
|---|---|
| Owner / Operator | LOMBART INSTRUMENT (#9001340) |
| Address | 5358 ROBIN HOOD RD, NORFOLK, VA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HKN |
| Regulation § (21 CFR) | 886.1770 |
| Proprietary names | Refractor |
Source: openFDA. Public-domain (CC0).