FDA inspection
Devicor Medical Products, Inc.: FDA inspection ending Aug 24, 2016
FDA inspection 983540 · No Action Indicated (NAI) · Blue Ash, OH
Key facts
| Inspection ID | 983540 |
|---|---|
| Firm | Devicor Medical Products, Inc. |
| FEI number | 3010339638 |
| Address | 4750 Lake Forest Dr Ste 120 |
| City | Blue Ash |
| State | OH |
| ZIP | 45242 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Aug 24, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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