FDA inspection
Ludlow Technical Products Canada, Ltd. (A Division of Cardinal Health LLC): FDA inspection ending Mar 21, 2013
FDA inspection 823780 · No Action Indicated (NAI) · Gananoque
Key facts
| Inspection ID | 823780 |
|---|---|
| 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 | 2013 |
| Inspection end date | Mar 21, 2013 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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