1Equipment and facility
Evaluation of production processes, equipment, and/or materials was inadequate.
Inspection Record
Sanofi Vaccines Canada Ltd. — Health Canada Inspection Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
2Deviation, CAPA, and investigation
Investigations into deviations, reports, and/or follow-up actions were inadequate.
3Equipment and facility
The design, construction, and/or location of the equipment did not allow adequate cleaning, sanitizing, and/or inspection of the equipment.
4Other quality system
The premises were not laid out and/or designed to ensure that production areas were adequately isolated and segregated.
About this record
Extracted automatically from the document of the Health Canada inspection on 2025-06-02. 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.
