FDA inspection
Alltech Medical Systems America Inc: FDA inspection ending Jul 29, 2019
FDA inspection 1097831 · Voluntary Action Indicated (VAI) · Solon, OH
Key facts
| Inspection ID | 1097831 |
|---|---|
| Firm | Alltech Medical Systems America Inc |
| FEI number | 3007138967 |
| Address | 28900 Fountain Pkwy Ste A |
| City | Solon |
| State | OH |
| ZIP | 44139 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Jul 29, 2019 |
| 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