FDA Device Establishments · JSON-LD · Markdown
FEI 1000305581 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 1000305581 |
|---|---|
| Owner / Operator | MICRO DIRECT, INC. (#9007705) |
| Address | 803 WEBSTER ST, LEWISTON, ME, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 2 |
| Product codes (top 20) | CCJ, JKT |
| Regulation § (21 CFR) | 868.1430, 862.3220 |
| Proprietary names | CO Screen; CO Check Pro |
Source: openFDA. Public-domain (CC0).