FDA Device Establishments · JSON-LD · Markdown
FEI 3006615210 · Repack or Relabel Medical Device Remanufacture Medical Device Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3006615210 |
|---|---|
| Owner / Operator | FORESEESON CUSTOM DISPLAYS, INC. (#10036004) |
| Address | 2210 E WINSTON RD, Anaheim, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KQM |
| Regulation § (21 CFR) | 878.4160 |
| Proprietary names | FS-P2604D; FM-C5501DV; FM-D5802DV; FS-P3102D; FS-A1904D(T); FS-P2602D(T); FS-L2702D(T); FS-P3102DS; WIS3000; FS-L3201D(T) |
Source: openFDA. Public-domain (CC0).