FDA Device Establishments · JSON-LD · Markdown
FEI 3000207346 · Manufacture Medical Device · Status: Active
| FEI Number | 3000207346 |
|---|---|
| Owner / Operator | J.P. GILBERT CO. (#9027898) |
| Address | 548 Mountain Rd, BOYERTOWN, PA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GKJ |
| Regulation § (21 CFR) | 864.5850 |
| Proprietary names | MINIPREP |
Source: openFDA. Public-domain (CC0).