1Equipment and facility
The design, construction, and/or location of the equipment did not allow adequate cleaning, sanitizing, and/or inspection of the equipment.
Inspection Record
PF Consumer Healthcare Canada ULC — Health Canada Inspection Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
2Other quality system
The availability, implementation, and/or quality of the written sanitation program was inadequate.
3Complaint and recall handling
The assessment, recording, follow-up, and/or investigation of complaints and/or other information about potentially defective products was inadequate.
4Equipment and facility
The usage logs for the equipment used for significant processing and/or testing operations were inadequate.
5Other quality system
The premises were not laid out and/or designed to ensure that production areas were adequately isolated and segregated.
6Deviation, CAPA, and investigation
The evaluation was inadequate for cases where there was a deviation from the norm and/or where products were on the borderline of the acceptable range.
7Quality unit oversight
The annual product quality review procedure was inadequate.
8Equipment 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.
About this record
Extracted automatically from the document of the Health Canada inspection on 2022-06-13. 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.
