FDA inspection
Boomerang Laboratories, Inc.: FDA inspection ending Nov 18, 2003
FDA inspection 302121 · Voluntary Action Indicated (VAI) · Spring Park, MN
Key facts
| Inspection ID | 302121 |
|---|---|
| Firm | Boomerang Laboratories, Inc. |
| FEI number | 3002842475 |
| Address | 4164 Shoreline Drive |
| City | Spring Park |
| State | MN |
| ZIP | 55384 |
| Fiscal year | 2004 |
| Inspection end date | Nov 18, 2003 |
| 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
- 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