FDA inspection
Midwest Eye Laboratories Inc: FDA inspection ending Dec 13, 2023
FDA inspection 1224877 · Voluntary Action Indicated (VAI) · Rochester, MN
Key facts
| Inspection ID | 1224877 |
|---|---|
| Firm | Midwest Eye Laboratories Inc |
| FEI number | 1000116180 |
| Address | 20 2nd Ave Sw |
| City | Rochester |
| State | MN |
| ZIP | 55902 |
| Country | United States |
| Fiscal year | 2024 |
| Inspection end date | Dec 13, 2023 |
| 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