FDA inspection
Iowa Corn Processors: FDA inspection ending Feb 16, 2016
FDA inspection 958902 · No Action Indicated (NAI) · Glidden, IA
Key facts
| Inspection ID | 958902 |
|---|---|
| Firm | Iowa Corn Processors |
| FEI number | 3002324308 |
| Address | 20481 Sycamore Ave |
| City | Glidden |
| State | IA |
| ZIP | 51443-8821 |
| Fiscal year | 2016 |
| Inspection end date | Feb 16, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Monitoring of Marketed Animal Drugs, Feeds, and Devices |
| Product type | Drugs |
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