Drug factory · FDA FEI 3001655239
Siegfried Grafton, Inc.
870 Badger Circle, Grafton, WI, United States
Problems found, fixed voluntarily at FDA's last inspection, Aug 21, 2026.
Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.
7 drug inspections on record since 2009: 2 with no problems, 5 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Nitrite Ion | Makes the active ingredient | Hope Pharmaceuticals | 60267-311 |
| Nitrite Ion and Thiosulfate Ion | Makes the active ingredient | Hope Pharmaceuticals | 60267-812 |
| Thiosulfate Ion | Makes the active ingredient | Hope Pharmaceuticals | 60267-705 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Aug 21, 2026 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Aug 14, 2024 | No problems found | Drug Quality Assurance | — |
| Jul 15, 2016 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Apr 4, 2013 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Jun 10, 2011 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Sep 20, 2010 | No problems found | Drug Quality Assurance | — |
| Dec 14, 2009 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
Registered with FDA for: analysis; api manufacture; particle size reduction.