FDA inspection
GF Health Products, Inc: FDA inspection ending Jun 12, 2012
FDA inspection 786634 · Voluntary Action Indicated (VAI) · Fond Du Lac, WI
Key facts
| Inspection ID | 786634 |
|---|---|
| Firm | GF Health Products, Inc |
| FEI number | 2183191 |
| Address | 336 Trowbridge Dr |
| City | Fond Du Lac |
| State | WI |
| ZIP | 54937 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Jun 12, 2012 |
| 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