FDA inspection
Avita Corporation: FDA inspection ending Oct 29, 2004
FDA inspection 358200 · Voluntary Action Indicated (VAI) · New Taipei City
Key facts
| Inspection ID | 358200 |
|---|---|
| Firm | Avita Corporation |
| FEI number | 3003272793 |
| Address | 9F, No. 78, Sec. 1,, GuangFu Rd. |
| City | New Taipei City |
| Fiscal year | 2005 |
| Inspection end date | Oct 29, 2004 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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