FDA inspection
Douglas Medical Products, Inc.: FDA inspection ending Sep 21, 2017
FDA inspection 1026575 · Voluntary Action Indicated (VAI) · Mundelein, IL
Key facts
| Inspection ID | 1026575 |
|---|---|
| Firm | Douglas Medical Products, Inc. |
| FEI number | 1000036860 |
| Address | 345 Dunbar Rd |
| City | Mundelein |
| State | IL |
| ZIP | 60060 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Sep 21, 2017 |
| 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