Inspection Record
View the regulator's official source The source document is always the basis for judgement.
The examination and/or approval of fabrication, packaging, labelling, testing, storage, and/or the transportation method and procedures by the person in charge of the quality control department before implementation was inadequate.
The handling of standard operating procedures for good manufacturing practices was inadequate.
The traceability, legibility, documentation, formatting, and/or the accuracy of records was inadequate.
The written procedures for recalls were inadequate.
Extracted automatically from the document of the Health Canada inspection on 2024-06-10. The source is available at the link above.
This is a record of that moment. 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 it as the current state; check the regulator's official announcements for the latest status.
Translation and classification are automated and may differ in nuance from the source.
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