FDA inspection
Ameditech Inc: FDA inspection ending May 12, 2016
FDA inspection 970516 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 970516 |
|---|---|
| Firm | Ameditech Inc |
| FEI number | 3003789989 |
| Address | 9940 Mesa Rim Rd |
| City | San Diego |
| State | CA |
| ZIP | 92121 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | May 12, 2016 |
| 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