FDA Device Establishments · JSON-LD · Markdown
FEI 3048183259 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3048183259 |
|---|---|
| Owner / Operator | AKICept, LLC (#10096182) |
| Address | 1210 Waterway Blvd, Indianapolis, IN, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 2 |
| Product codes (top 20) | KNW, FCG |
| Regulation § (21 CFR) | 876.1075 |
Source: openFDA. Public-domain (CC0).