The availability, content and/or maintenance of the quality agreements between the supplier, fabricator, tester, packager, labeller, distributor, importer, and/or wholesaler was inadequate.
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Health Canada Equipment and facility findings
by this agency in this category 1,463 findings drawn from 997 published documents. The most recent cases are below; the full set is in search.
See all Health Canada Equipment and facility findingsCompanies with the most findings
Recent findings
A preventative maintenance system had not been established for the equipment used in significant processing and/or testing operations
See every finding in this document View the regulator's official sourceEvaluation of production processes, equipment, and/or materials was inadequate.
See every finding in this document View the regulator's official sourceThe establishment and/or the maintenance of a data governance plan was inadequate.
See every finding in this document View the regulator's official sourceThe training of personnel in good manufacturing practices and/or the maintenance of records was inadequate.
See every finding in this document View the regulator's official sourceThe system for reviewing, revising, and approving standard operating procedures was inadequate. The maintenance of records was inadequate.
See every finding in this document View the regulator's official sourceOther agencies
These findings are a record of the moment each document was published. Inspection findings are usually followed by the company's response and corrective action, but this page does not know how that turned out — do not read them as the current state; check the regulator's official announcements for the latest status. Counts are measured from public data as of 2026-10-20, and findings are extracted automatically from the regulator's published documents. “View official source” on each case links directly to that document.
