FDA Device Establishments · JSON-LD · Markdown
FEI 3008384335 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3008384335 |
|---|---|
| Owner / Operator | GFA Production Xiamen Co., Ltd. (#9073017) |
| Address | #20 HuLi Industrial Park, Mei Xi Dao, Tong An, Xiamen Fujian, 361100, CN |
| Mandatory US Agent | Registrar Corp |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KXF |
| Regulation § (21 CFR) | 880.6025 |
Source: openFDA. Public-domain (CC0).