FDA inspection
Custom Foam Systems Ltd.: FDA inspection ending Nov 19, 2015
FDA inspection 952123 · Voluntary Action Indicated (VAI) · Kitchener
Key facts
| Inspection ID | 952123 |
|---|---|
| Firm | Custom Foam Systems Ltd. |
| FEI number | 3002668219 |
| Address | 360 Trillium Dr |
| City | Kitchener |
| Country | Canada |
| Fiscal year | 2016 |
| Inspection end date | Nov 19, 2015 |
| 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