1Computer system validation
The calibration, inspection, and/or qualification of the equipment, including computerized systems, was inadequate. The preventative maintenance and repair of the equipment was inadequate.
Inspection Record
Air Liquide Canada Inc. — Health Canada Inspection Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
2Quality unit oversight
The annual product quality review procedure was inadequate.
3Equipment and facility
The maintenance of personnel records was inadequate.
4Other quality system
The handling of standard operating procedures for good manufacturing practices was inadequate.
5Laboratory and QC controls
The quality control department did not undertake all of the required activities.
6Equipment and facility
The maintenance of records was inadequate.
7Equipment and facility
The premises were not designed, constructed, and/or maintained to prevent the entry of pests and/or foreign material into the building.
About this record
Extracted automatically from the document of the Health Canada inspection on 2026-06-24. 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.
