FDA inspection
Medline Industries, Inc: FDA inspection ending May 26, 2005
FDA inspection 380358 · Voluntary Action Indicated (VAI) · Mundelein, IL
Key facts
| Inspection ID | 380358 |
|---|---|
| Firm | Medline Industries, Inc |
| FEI number | 1000138386 |
| Address | 1200 Townline Rd |
| City | Mundelein |
| State | IL |
| ZIP | 60060-4448 |
| Fiscal year | 2005 |
| Inspection end date | May 26, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
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