FDA Device Establishments · JSON-LD · Markdown
FEI 3004586080 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3004586080 |
|---|---|
| Owner / Operator | KLEEN TEST PRODUCTS CORPORATION (#2122794) |
| Address | 1611 S SUNSET RD, Port Washington, WI, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FRL |
| Regulation § (21 CFR) | 880.5300 |
Source: openFDA. Public-domain (CC0).