FDA Device Establishments · JSON-LD · Markdown
FEI 3014267863 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3014267863 |
|---|---|
| Owner / Operator | Acuity Pro, Inc. (#10056694) |
| Address | 920 N Main St, Elk City, OK, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HOX |
| Regulation § (21 CFR) | 886.1150 |
| Proprietary names | Acuity Pro |
Source: openFDA. Public-domain (CC0).