The master production documents were inadequate. The handling of raw materials, products, or packaging materials in keeping with pre-approved written procedures or instructions was inadequate.
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Health Canada Material and supplier control findings
by this agency in this category 408 findings drawn from 319 published documents. The most recent cases are below; the full set is in search.
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Recent findings
The sampling plan for raw materials was inadequate.
See every finding in this document View official sourceThe segregation, rotation of stock, and/or the transportation of raw materials, packaging materials, intermediates, bulk drugs, and/or finished products was inadequate.
View official sourceThe premises were not laid out and/or designed for an optimal flow of personnel and/or materials to prevent cross-contamination and/or mix-ups between products.
See every finding in this document View official sourceThe premises were not laid out and/or designed for an optimal flow of personnel and/or materials to prevent cross-contamination and/or mix-ups between products.
See every finding in this document View official sourceThe control of quarantine areas was inadequate. The segregation, rotation of stock, and/or the transportation of raw materials, packaging materials, intermediates, bulk drugs, and/or finished products was inadequate.
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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 2026-09-04, and findings are extracted automatically from the regulator's published documents. “View official source” on each case links directly to that document.
