FDA inspection
Ioditech Inc: FDA inspection ending Aug 5, 2003
FDA inspection 286625 · Official Action Indicated (OAI) · Kansas City, MO
Key facts
| Inspection ID | 286625 |
|---|---|
| Firm | Ioditech Inc |
| FEI number | 1910085 |
| Address | 951 N Topping Ave |
| City | Kansas City |
| State | MO |
| ZIP | 64120-1991 |
| Fiscal year | 2003 |
| Inspection end date | Aug 5, 2003 |
| Classification | Official Action Indicated (OAI) |
| Project area | Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug 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Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev |
| 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