FDA inspection
Apheresis Technologies, Inc.: FDA inspection ending May 24, 2004
FDA inspection 327541 · Voluntary Action Indicated (VAI) · Palm Harbor, FL
Key facts
| Inspection ID | 327541 |
|---|---|
| Firm | Apheresis Technologies, Inc. |
| FEI number | 1000113717 |
| Address | 612 Florida Ave |
| City | Palm Harbor |
| State | FL |
| ZIP | 34683-5459 |
| Fiscal year | 2004 |
| Inspection end date | May 24, 2004 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None 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