FDA inspection
Nidek Medical Products Inc: FDA inspection ending Sep 30, 2008
FDA inspection 539075 · Official Action Indicated (OAI) · Birmingham, AL
Key facts
| Inspection ID | 539075 |
|---|---|
| Firm | Nidek Medical Products Inc |
| FEI number | 1039215 |
| Address | 3949 Valley East Industrial Dr |
| City | Birmingham |
| State | AL |
| ZIP | 35217-1838 |
| Fiscal year | 2008 |
| Inspection end date | Sep 30, 2008 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
| Warning letter | 42638 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes 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