FDA inspection
AMPLIFON: FDA inspection ending Jun 20, 2002
FDA inspection 224344 · Voluntary Action Indicated (VAI) · Milan
Key facts
| Inspection ID | 224344 |
|---|---|
| Firm | AMPLIFON |
| FEI number | 3002806418 |
| Address | Via Giuseppe Ripamonti 133 |
| City | Milan |
| Fiscal year | 2002 |
| Inspection end date | Jun 20, 2002 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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