FDA inspection
Gannon Elevator Company: FDA inspection ending Jan 16, 2003
FDA inspection 262319 · Kimball, MN
Key facts
| Inspection ID | 262319 |
|---|---|
| Firm | Gannon Elevator Company |
| FEI number | 2115321 |
| Address | 40 Linden Ave W |
| City | Kimball |
| State | MN |
| ZIP | 55353 |
| Fiscal year | 2003 |
| Inspection end date | Jan 16, 2003 |
| 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
- 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