FDA inspection
Ludlow Technical Products Canada, Ltd. (A Division of Cardinal Health LLC): FDA inspection ending Jan 12, 2023
FDA inspection 1198500 · No Action Indicated (NAI) · Gananoque
Key facts
| Inspection ID | 1198500 |
|---|---|
| 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 | 2023 |
| Inspection end date | Jan 12, 2023 |
| Classification | No Action Indicated (NAI) |
| Project area | Project Evaluation: 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