Health Canada citation
FDA s.21 - prescribed standards
Health Canada inspection citation · Food and Drugs Act (R.S.C. 1985, c. F-27)
Key facts
| Requirement | FDA s.21 - prescribed standards |
|---|---|
| Regulation | Food and Drugs Act (R.S.C. 1985, c. F-27) |
| Example observations (excerpt) | medical devices were labelled, packaged, sold or advertised in a manner which could be mistaken for conformance to a prescribed standard. risk 2: medical devices were labelled, packaged, sold or advertised in a manner which could be mistaken for conformance to a prescribed standard. |
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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