FDA inspection
Norfolk Medical Products Inc: FDA inspection ending Mar 4, 2003
FDA inspection 261211 · Official Action Indicated (OAI) · Skokie, IL
Key facts
| Inspection ID | 261211 |
|---|---|
| Firm | Norfolk Medical Products Inc |
| FEI number | 1450392 |
| Address | 7350 Ridgeway Ave |
| City | Skokie |
| State | IL |
| ZIP | 60076-4027 |
| Fiscal year | 2003 |
| Inspection end date | Mar 4, 2003 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
| Warning letter | UCM147517 |
At a glance
- 10–99 Citations
- 1–9 Posted citations
- Yes 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