FDA inspection
Diamond Products Company: FDA inspection ending May 15, 2001
FDA inspection 75477 · No Action Indicated (NAI) · Saint Paul, MN
Key facts
| Inspection ID | 75477 |
|---|---|
| Firm | Diamond Products Company |
| FEI number | 2111106 |
| Address | 310 5th St E |
| City | Saint Paul |
| State | MN |
| ZIP | 55101-1610 |
| Fiscal year | 2001 |
| Inspection end date | May 15, 2001 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None 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