FDA inspection
Isomedix Operations Inc.: FDA inspection ending Sep 26, 2007
FDA inspection 492961 · No Action Indicated (NAI) · Coon Rapids, MN
Key facts
| Inspection ID | 492961 |
|---|---|
| Firm | Isomedix Operations Inc. |
| FEI number | 2183744 |
| Address | 380 90th Ave Nw |
| City | Coon Rapids |
| State | MN |
| ZIP | 55433-5826 |
| Fiscal year | 2007 |
| Inspection end date | Sep 26, 2007 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: 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
- 10–99 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