FDA inspection
Beckman Coulter, Inc.: FDA inspection ending Dec 30, 2009
FDA inspection 640328 · No Action Indicated (NAI) · Chaska, MN
Key facts
| Inspection ID | 640328 |
|---|---|
| Firm | Beckman Coulter, Inc. |
| FEI number | 2122870 |
| Address | 1000 Lake Hazeltine Dr |
| City | Chaska |
| State | MN |
| ZIP | 55318-1037 |
| Fiscal year | 2010 |
| Inspection end date | Dec 30, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No 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