FDA inspection
FlexDex Inc.: FDA inspection ending Jun 22, 2017
FDA inspection 1015191 · Voluntary Action Indicated (VAI) · Brighton, MI
Key facts
| Inspection ID | 1015191 |
|---|---|
| Firm | FlexDex Inc. |
| FEI number | 3012046682 |
| Address | 10421 Citation Dr Ste 900 |
| City | Brighton |
| State | MI |
| ZIP | 48116 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Jun 22, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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