FDA inspection
Apheresis Technologies, Inc.: FDA inspection ending Apr 1, 2009
FDA inspection 573802 · Voluntary Action Indicated (VAI) · Palm Harbor, FL
Key facts
| Inspection ID | 573802 |
|---|---|
| Firm | Apheresis Technologies, Inc. |
| FEI number | 1000113717 |
| Address | 612 Florida Ave |
| City | Palm Harbor |
| State | FL |
| ZIP | 34683 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Apr 1, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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