Health Canada citation
MDR s.75(a)-(c) - specific labelling
Health Canada inspection citation · Medical Devices Regulations (SOR/98-282)
Key facts
| Requirement | MDR s.75(a)-(c) - specific labelling |
|---|---|
| Regulation | Medical Devices Regulations (SOR/98-282) |
| Example observations (excerpt) | risk 2: the company imported or sold devices without a label specifying the device was custom-made. risk 2: the company imported or sold devices without a label specifying the device was intended for special access use. risk 3: the company imported or sold devices without a label specifying the… |
At a glance
- 1–9 Health Canada inspections citing this requirement
- No Among the 20 most-cited Health Canada requirements
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Health Canada regulation sections cited in inspections
Health Canada inspection reports cite the section of the Food and Drug Regulations, Medical Devices Regulations or Blood Regulations behind each observation. This page counts the published inspections that cite the requirement.
Source: Health Canada, Drug and Health Product Inspections; citation counts by Orca1. Contains information licensed under the Open Government Licence – Canada
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