FDA inspection
Midwest Eye Laboratories Woodbury, LLC: FDA inspection ending Mar 11, 2008
FDA inspection 509553 · No Action Indicated (NAI) · Saint Paul, MN
Key facts
| Inspection ID | 509553 |
|---|---|
| Firm | Midwest Eye Laboratories Woodbury, LLC |
| FEI number | 2183831 |
| Address | 7582 Currell Blvd Ste 109 |
| City | Saint Paul |
| State | MN |
| ZIP | 55125-8212 |
| Fiscal year | 2008 |
| Inspection end date | Mar 11, 2008 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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