FDA inspection
Asahi Kasei Medical America Inc Memphis Distribution Center: FDA inspection ending Jan 11, 2018
FDA inspection 1037688 · Voluntary Action Indicated (VAI) · Glenview, IL
Key facts
| Inspection ID | 1037688 |
|---|---|
| Firm | Asahi Kasei Medical America Inc Memphis Distribution Center |
| FEI number | 3006396296 |
| Address | 1855 Elmdale Ave |
| City | Glenview |
| State | IL |
| ZIP | 60026 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Jan 11, 2018 |
| 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