FDA inspection
Topiderm Inc.: FDA inspection ending May 13, 2014
FDA inspection 878235 · Voluntary Action Indicated (VAI) · Amityville, NY
Key facts
| Inspection ID | 878235 |
|---|---|
| Firm | Topiderm Inc. |
| FEI number | 2432734 |
| Address | 5200 New Horizons Blvd |
| City | Amityville |
| State | NY |
| ZIP | 11701 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | May 13, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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