FDA inspection
Confluent Medical Technologies, Inc.: FDA inspection ending Mar 29, 2006
FDA inspection 420015 · Voluntary Action Indicated (VAI) · Fremont, CA
Key facts
| Inspection ID | 420015 |
|---|---|
| Firm | Confluent Medical Technologies, Inc. |
| FEI number | 3007635982 |
| Address | 47533 Westinghouse Dr |
| City | Fremont |
| State | CA |
| ZIP | 94539-7463 |
| Fiscal year | 2006 |
| Inspection end date | Mar 29, 2006 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
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