FDA inspection
Midwest Eye Laboratories Sioux Falls, LLC: FDA inspection ending Feb 15, 2018
FDA inspection 1042349 · No Action Indicated (NAI) · Sioux Falls, SD
Key facts
| Inspection ID | 1042349 |
|---|---|
| Firm | Midwest Eye Laboratories Sioux Falls, LLC |
| FEI number | 1000116181 |
| Address | 1606 S Western Ave Ste C |
| City | Sioux Falls |
| State | SD |
| ZIP | 57110 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Feb 15, 2018 |
| 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