FDA inspection
Norfolk Medical Products Inc: FDA inspection ending Mar 22, 2001
FDA inspection 67605 · No Action Indicated (NAI) · Skokie, IL
Key facts
| Inspection ID | 67605 |
|---|---|
| Firm | Norfolk Medical Products Inc |
| FEI number | 1450392 |
| Address | 7350 Ridgeway Ave |
| City | Skokie |
| State | IL |
| ZIP | 60076-4027 |
| Fiscal year | 2001 |
| Inspection end date | Mar 22, 2001 |
| Classification | No Action Indicated (NAI) |
| 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