FDA inspection
Woodward Iodine Corporation: FDA inspection ending Aug 26, 2003
FDA inspection 292617 · Voluntary Action Indicated (VAI) · Woodward, OK
Key facts
| Inspection ID | 292617 |
|---|---|
| Firm | Woodward Iodine Corporation |
| FEI number | 1626455 |
| Address | 8 Mi North Hwy 34,3 Miles East EW-32, Po Box 1245 |
| City | Woodward |
| State | OK |
| ZIP | 73802-1245 |
| Fiscal year | 2003 |
| Inspection end date | Aug 26, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| 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
- 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