1Deviation, CAPA, and investigation
Investigations into deviations, reports, and/or follow-up actions were inadequate.
Inspection Record
Thunder Bay Regional Health Sciences Centre — Health Canada Inspection Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
2Equipment and facility
The availability, content and/or maintenance of the quality agreements between the supplier, fabricator, tester, packager, labeller, distributor, importer, and/or wholesaler was inadequate.
3Equipment and facility
The validation of equipment or the planned maintenance of equipment was inadequate.
4Contamination control
The sanitation programs were not adequately designed to identify and/or reduce the risks of contamination.
5Other quality system
The implementation of a self-inspection program was inadequate.
6Aseptic processing and sterility assurance
The operators'aseptic practices were inadequate to maintain sterility. Evaluation of production processes, equipment, and/or materials was inadequate. The environmental standards were inadequate in order to minimise particular or microbial contamination of aseptic or clean areas.
7Laboratory and QC controls
The creation, maintenance, processing, and/or review of laboratory data was inadequate.
About this record
Extracted automatically from the document of the Health Canada inspection on 2026-06-01. 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.
