FDA inspection
Aea Srl: FDA inspection ending Jan 10, 2020
FDA inspection 1116630 · Voluntary Action Indicated (VAI) · Maiolati Spontini
Key facts
| Inspection ID | 1116630 |
|---|---|
| Firm | Aea Srl |
| FEI number | 3006571738 |
| Address | Via Monteschiavo 3, De Maiolati |
| City | Maiolati Spontini |
| Country | Italy |
| Fiscal year | 2020 |
| Inspection end date | Jan 10, 2020 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- None 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