FDA inspection
New Genesis/Monticello Drug, LLC: FDA inspection ending Jul 20, 2000
FDA inspection 30461 · Voluntary Action Indicated (VAI) · Jacksonville, FL
Key facts
| Inspection ID | 30461 |
|---|---|
| Firm | New Genesis/Monticello Drug, LLC |
| FEI number | 1012303 |
| Address | 2801 Lorimier Ter |
| City | Jacksonville |
| State | FL |
| ZIP | 32207-4146 |
| Fiscal year | 2000 |
| Inspection end date | Jul 20, 2000 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No 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