FDA inspection
Asahi Intecc Usa Inc: FDA inspection ending Jun 1, 2023
FDA inspection 1206900 · Voluntary Action Indicated (VAI) · Tustin, CA
Key facts
| Inspection ID | 1206900 |
|---|---|
| Firm | Asahi Intecc Usa Inc |
| FEI number | 3004718255 |
| Address | 3002 Dow Ave Ste 212 |
| City | Tustin |
| State | CA |
| ZIP | 92780 |
| Country | United States |
| Fiscal year | 2023 |
| Inspection end date | Jun 1, 2023 |
| 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