FDA Device Establishments · JSON-LD · Markdown
FEI 1000112835 · Manufacture Medical Device · Status: Active
| FEI Number | 1000112835 |
|---|---|
| Owner / Operator | AlcoPro Inc (#10033291) |
| Address | 1626 Downtown West Boulevard, Knoxville, TN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DJZ |
| Regulation § (21 CFR) | 862.3050 |
| Proprietary names | BreathIQ; Alco-Breath Tube; CheckPoint |
Source: openFDA. Public-domain (CC0).