FDA inspection
Weiman Products, LLC: FDA inspection ending Jan 10, 2018
FDA inspection 1037374 · Voluntary Action Indicated (VAI) · Gurnee, IL
Key facts
| Inspection ID | 1037374 |
|---|---|
| Firm | Weiman Products, LLC |
| FEI number | 1416404 |
| Address | 755 Tri State Pkwy |
| City | Gurnee |
| State | IL |
| ZIP | 60031 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Jan 10, 2018 |
| 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