FDA inspection
Dermarite Industries, LLC.: FDA inspection ending Oct 9, 2003
FDA inspection 296058 · Voluntary Action Indicated (VAI) · North Bergen, NJ
Key facts
| Inspection ID | 296058 |
|---|---|
| Firm | Dermarite Industries, LLC. |
| FEI number | 1000526900 |
| Address | 7777 W Side Ave |
| City | North Bergen |
| State | NJ |
| ZIP | 07047-6436 |
| Fiscal year | 2004 |
| Inspection end date | Oct 9, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 10–99 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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