FDA inspection
Roth, Sanford H Md: FDA inspection ending Mar 31, 2003
FDA inspection 266162 · Voluntary Action Indicated (VAI) · Phoenix, AZ
Key facts
| Inspection ID | 266162 |
|---|---|
| Firm | Roth, Sanford H Md |
| FEI number | 2080779 |
| Address | 3330 N 2nd St Ste 601 |
| City | Phoenix |
| State | AZ |
| ZIP | 85012-2395 |
| Fiscal year | 2003 |
| Inspection end date | Mar 31, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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