FDA inspection
Hart Medical Equipment: FDA inspection ending May 16, 2012
FDA inspection 781735 · Voluntary Action Indicated (VAI) · Grand Blanc, MI
Key facts
| Inspection ID | 781735 |
|---|---|
| Firm | Hart Medical Equipment |
| FEI number | 1832201 |
| Address | 1000 Health Park Blvd |
| City | Grand Blanc |
| State | MI |
| ZIP | 48439 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | May 16, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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