FDA inspection
IKI Mfg Co., Inc: FDA inspection ending Aug 17, 2007
FDA inspection 485032 · Voluntary Action Indicated (VAI) · Edgerton, WI
Key facts
| Inspection ID | 485032 |
|---|---|
| Firm | IKI Mfg Co., Inc |
| FEI number | 2111719 |
| Address | 107 Maple Court/Site |
| City | Edgerton |
| State | WI |
| ZIP | 53534 |
| Fiscal year | 2007 |
| Inspection end date | Aug 17, 2007 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| 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