FDA inspection
GreenMark Biomedical Inc.: FDA inspection ending Apr 18, 2025
FDA inspection 1267215 · Voluntary Action Indicated (VAI) · Ann Arbor, MI
Key facts
| Inspection ID | 1267215 |
|---|---|
| Firm | GreenMark Biomedical Inc. |
| FEI number | 3020856747 |
| Address | 1600 Huron Pwy Bdg 520 2nd Floor |
| City | Ann Arbor |
| State | MI |
| ZIP | 48109 |
| Country | United States |
| Fiscal year | 2025 |
| Inspection end date | Apr 18, 2025 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data