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 implementation and/or the effectiveness of the sanitation program in preventing unsanitary conditions was inadequate.
The specifications for any packaging materials were incomplete or inadequate.
Critical production processes were not validated. The recorded information or details were inadequate.
The premises were not designed, constructed, operated, and/or maintained to prevent contamination. The doors, windows, walls, ceilings, and/or floors were inadequate. The temperature and/or humidity control was inadequate.
Dedicated production equipment (used solely for specific purposes) was not provided where appropriate and/or required.
The education, experience, and/or oversight of the individual in charge of the quality control department was inadequate.
Extracted automatically from the document of the Health Canada inspection on 2025-10-28. 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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