FDA inspection
Midmark Corporation: FDA inspection ending Aug 22, 2017
FDA inspection 1026007 · No Action Indicated (NAI) · Buffalo Grove, IL
Key facts
| Inspection ID | 1026007 |
|---|---|
| Firm | Midmark Corporation |
| FEI number | 3000210017 |
| Address | 1001 Asbury Dr |
| City | Buffalo Grove |
| State | IL |
| ZIP | 60089 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Aug 22, 2017 |
| 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