FDA inspection
Ionetix Corporation: FDA inspection ending Jul 12, 2019
FDA inspection 1097847 · Voluntary Action Indicated (VAI) · Kansas City, KS
Key facts
| Inspection ID | 1097847 |
|---|---|
| Firm | Ionetix Corporation |
| FEI number | 3015265824 |
| Address | 3901 Rainbow Blvd Rm B701 |
| City | Kansas City |
| State | KS |
| ZIP | 66160-8500 |
| Fiscal year | 2019 |
| Inspection end date | Jul 12, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Generic Drug Evaluation |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 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