FDA inspection
Nostrum Laboratories Inc: FDA inspection ending Oct 28, 1999
FDA inspection 4186 · Voluntary Action Indicated (VAI) · Kansas City, MO
Key facts
| Inspection ID | 4186 |
|---|---|
| Firm | Nostrum Laboratories Inc |
| FEI number | 1930436 |
| Address | 1800 N Topping Ave |
| City | Kansas City |
| State | MO |
| ZIP | 64120-1228 |
| Fiscal year | 2000 |
| Inspection end date | Oct 28, 1999 |
| 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
- 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