FDA Device Establishments · JSON-LD · Markdown
FEI 3013687630 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3013687630 |
|---|---|
| Owner / Operator | Meloq AB (#10056849) |
| Address | Brannkyrkagatan 72, Stockholm, 118 23, SE |
| Mandatory US Agent | J & D CAMPBELL ASSOCIATES, INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KQX |
| Regulation § (21 CFR) | 888.1500 |
Source: openFDA. Public-domain (CC0).