FDA inspection
Ludlow Technical Products Canada, Ltd. (A Division of Cardinal Health LLC): FDA inspection ending Jan 28, 2016
FDA inspection 961724 · Voluntary Action Indicated (VAI) · Gananoque
Key facts
| Inspection ID | 961724 |
|---|---|
| Firm | Ludlow Technical Products Canada, Ltd. (A Division of Cardinal Health LLC) |
| FEI number | 3003491392 |
| Address | 215 Herbert St |
| City | Gananoque |
| Country | Canada |
| Fiscal year | 2016 |
| Inspection end date | Jan 28, 2016 |
| 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