FDA inspection
Murata Vios Inc.: FDA inspection ending Apr 25, 2024
FDA inspection 1237095 · Voluntary Action Indicated (VAI) · Duluth, GA
Key facts
| Inspection ID | 1237095 |
|---|---|
| Firm | Murata Vios Inc. |
| FEI number | 3015180161 |
| Address | 3079 Premiere Pkwy Ste 140 |
| City | Duluth |
| State | GA |
| ZIP | 30097 |
| Country | United States |
| Fiscal year | 2024 |
| Inspection end date | Apr 25, 2024 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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