FDA inspection
Haven Innovation, Inc.: FDA inspection ending Dec 17, 2015
FDA inspection 952747 · Voluntary Action Indicated (VAI) · Grand Haven, MI
Key facts
| Inspection ID | 952747 |
|---|---|
| Firm | Haven Innovation, Inc. |
| FEI number | 3008879703 |
| Address | 1705 Eaton Dr |
| City | Grand Haven |
| State | MI |
| ZIP | 49417 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Dec 17, 2015 |
| 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