FDA Device Establishments · JSON-LD · Markdown
FEI 3003701733 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3003701733 |
|---|---|
| Owner / Operator | KIMBERLY-CLARK CORPORATION (#9001775) |
| Address | 2100 WINCHESTER RD., NEENAH, WI, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HEB |
| Regulation § (21 CFR) | 884.5470 |
| Proprietary names | U by Kotex |
Source: openFDA. Public-domain (CC0).