The operators'aseptic practices were inadequate to maintain sterility.
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Health Canada Aseptic processing and sterility assurance findings
by this agency in this category 274 findings drawn from 140 published documents. The most recent cases are below; the full set is in search.
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Recent findings
Evaluation of production processes, equipment, and/or materials was inadequate. The operators'aseptic practices were inadequate to maintain sterility.
See every finding in this document View the regulator's official sourceThe samples taken for sterility testing were not representative of the whole batch.
See every finding in this document View the regulator's official sourceThe environmental standards were inadequate in order to minimise particular or microbial contamination of aseptic or clean areas.
See every finding in this document View the regulator's official sourceThe environmental standards were inadequate in order to minimise particular or microbial contamination of aseptic or clean areas. The quality control department did not undertake all of the required activities.
See every finding in this document View the regulator's official sourceThe sampling procedure was inadequate for microbiological monitoring in processing areas or aseptic areas. The company did not set appropriate alert and action limits for the results of particulate and microbiological monitoring.
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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 2026-10-20, and findings are extracted automatically from the regulator's published documents. “View official source” on each case links directly to that document.
