1Laboratory and QC controls
The validation and/or the documentation of test methods 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
2Complaint and recall handling
The quality control department's handling of complaints and/or information received about drug quality was inadequate.
3Computer system validation
The calibration, inspection, and/or qualification of the equipment, including computerized systems, was inadequate.
4Training and personnel
The health examinations of personnel (pre-employment and/or ongoing) were inadequate.
5Other quality system
The receipt, preparation, and/or handling of reagents and culture media was inadequate.
6Other quality system
Periodic confirmatory testing was not conducted.
7Other quality system
The handling of standard operating procedures for good manufacturing practices was inadequate.
About this record
Extracted automatically from the document of the Health Canada inspection on 2025-10-08. 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.
