FDA Device Establishments · JSON-LD · Markdown
FEI 3029960285 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3029960285 |
|---|---|
| Owner / Operator | GuideStar Medical Devices Inc. (#10089132) |
| Address | 201-2067 Cadboro Bay Rd, Victoria British Columbia, V8R5G4, CA |
| Mandatory US Agent | Lean RAQA, LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FMF |
| Regulation § (21 CFR) | 880.5860 |
| Proprietary names | EpiZact |
Source: openFDA. Public-domain (CC0).