Drug factory · FDA FEI 1824624
Aurorium LLC
215 North Centennial Street, Zeeland, MI, United States
Problems found, fixed voluntarily at FDA's last inspection, Jul 31, 2025.
Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.
6 drug inspections on record since 2010: 0 with no problems, 6 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Zinc Cation | Makes the active ingredient | Eton Pharmaceuticals, Inc. | 71863-124, 71863-125 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Jul 31, 2025 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Apr 9, 2019 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Jul 11, 2014 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Jun 15, 2012 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Jun 21, 2011 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Aug 27, 2010 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
Registered with FDA for: api manufacture.