FDA inspection
Fziomed Inc: FDA inspection ending Aug 14, 2006
FDA inspection 438367 · Voluntary Action Indicated (VAI) · San Luis Obispo, CA
Key facts
| Inspection ID | 438367 |
|---|---|
| Firm | Fziomed Inc |
| FEI number | 3004474407 |
| Address | 231 Bonetti Dr |
| City | San Luis Obispo |
| State | CA |
| ZIP | 93401-7376 |
| Fiscal year | 2006 |
| Inspection end date | Aug 14, 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