FDA inspection
Wykle, Inc.: FDA inspection ending May 10, 2019
FDA inspection 1089189 · Voluntary Action Indicated (VAI) · Carson City, NV
Key facts
| Inspection ID | 1089189 |
|---|---|
| Firm | Wykle, Inc. |
| FEI number | 2020703 |
| Address | 2222 College Pkwy |
| City | Carson City |
| State | NV |
| ZIP | 89706 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | May 10, 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