FDA inspection
Hu-Friedy Mfg Co, Inc.: FDA inspection ending Mar 3, 2009
FDA inspection 570891 · No Action Indicated (NAI) · Northbrook, IL
Key facts
| Inspection ID | 570891 |
|---|---|
| Firm | Hu-Friedy Mfg Co, Inc. |
| FEI number | 1416605 |
| Address | 3232 N Rockwell St |
| City | Northbrook |
| State | IL |
| ZIP | 60062 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Mar 3, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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
- 10–99 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