FDA inspection
Ioditech Inc: FDA inspection ending Jul 19, 2005
FDA inspection 388451 · Official Action Indicated (OAI) · Kansas City, MO
Key facts
| Inspection ID | 388451 |
|---|---|
| Firm | Ioditech Inc |
| FEI number | 1910085 |
| Address | 951 N Topping Ave |
| City | Kansas City |
| State | MO |
| ZIP | 64120-1991 |
| Fiscal year | 2005 |
| Inspection end date | Jul 19, 2005 |
| Classification | Official Action Indicated (OAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 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