FDA inspection
Kellanova Manufacturing LLC.: FDA inspection ending Feb 9, 2017
FDA inspection 1000470 · No Action Indicated (NAI) · Grand Rapids, MI
Key facts
| Inspection ID | 1000470 |
|---|---|
| Firm | Kellanova Manufacturing LLC. |
| FEI number | 1810657 |
| Address | 310 28th St SE |
| City | Grand Rapids |
| State | MI |
| ZIP | 49548 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Feb 9, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Foodborne Biological Hazards |
| Product type | Food/Cosmetics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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