FDA inspection
Triple K Manufacturing Company, Inc.: FDA inspection ending Feb 17, 2012
FDA inspection 768772 · Shenandoah, IA
Key facts
| Inspection ID | 768772 |
|---|---|
| Firm | Triple K Manufacturing Company, Inc. |
| FEI number | 1911030 |
| Address | 4193 Airport Rd |
| City | Shenandoah |
| State | IA |
| ZIP | 51601 |
| Fiscal year | 2012 |
| Inspection end date | Feb 17, 2012 |
| Product type | Food/Cosmetics |
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