FDA Device Establishments · JSON-LD · Markdown
FEI 3006408818 · Reprocess Single-Use Device Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Repack or Relabel Medical Device · Status: Active
| FEI Number | 3006408818 |
|---|---|
| Owner / Operator | ING Source, LLC (#10040165) |
| Address | 1340 14th Ave CT SW, Hickory, NC, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | IQI |
| Regulation § (21 CFR) | 890.3475 |
| Proprietary names | ES6; TT3; ES3; KS7+; WS6; KS7; QS4; KS8 |
Source: openFDA. Public-domain (CC0).