Firm Record
Air Liquide Canada Inc. findings history
161 findings from 30 inspection documents published by regulators. Each row below says what its date means.
Areas cited
Other quality systemEquipment and facilityRegulatory reporting and change controlLaboratory and QC controlsCleaning validationComputer system validationTraining and personnelDeviation, CAPA, and investigationQuality unit oversightComplaint and recall handlingMaterial and supplier controlLabeling and packagingContamination control
Published inspection documents
2026-06-24
Health Canada
7 findingsComputer system validation · Quality unit oversight · Equipment and facility · Other quality system · Laboratory and QC controls The calibration, inspection, and/or qualification of the equipment, including computerized systems, was inadequate. The preventative maintenance and repair of the equipment was inadequate.
2026-03-02
Health Canada
3 findingsEquipment and facility · Deviation, CAPA, and investigation · Other quality system The maintenance of records was inadequate.
2025-11-06
Health Canada
5 findingsEquipment and facility · Other quality system · Material and supplier control The preventative maintenance and repair of the equipment was inadequate.
2025-11-03
Health Canada
5 findingsOther quality system · Material and supplier control · Equipment and facility The recorded information or details were inadequate.
2025-10-30
Health Canada
5 findingsMaterial and supplier control · Other quality system · Equipment and facility The segregation, rotation of stock, and/or the transportation of raw materials, packaging materials, intermediates, bulk drugs, and/or finished products was inadequate. The control of quarantine areas was inadequate.
2025-10-08
Health Canada
7 findingsLaboratory and QC controls · Complaint and recall handling · Computer system validation · Training and personnel · Other quality system The validation and/or the documentation of test methods was inadequate.
2025-02-25
Health Canada
6 findingsLaboratory and QC controls · Regulatory reporting and change control · Training and personnel · Other quality system The quality control department did not approve, sign, and/or date the good manufacturing practices documents and/or the standard operating procedures.
2024-11-18
Health Canada
4 findingsEquipment and facility · Other quality system The equipment was not set-up, designed, operated, stored, and/or maintained to prevent potential contamination of drugs by other drugs and/or by foreign material. The usage logs for the equipment used for significant processing and/or testing operations were inadequate.
2024-10-17
Health Canada
3 findingsOther quality system · Equipment and facility · Laboratory and QC controls The premises were not laid out and/or designed to ensure that production areas were adequately isolated and segregated.
2024-10-16
Health Canada
4 findingsOther quality system The implementation of a self-inspection program was inadequate.
2024-10-16
Health Canada
7 findingsOther quality system · Computer system validation · Laboratory and QC controls · Quality unit oversight · Equipment and facility · Labeling and packaging · Contamination control The controls were inadequate for creating, modifying, reviewing, storing, and/or retrieving records.
2024-04-12
Health Canada
5 findingsOther quality system · Laboratory and QC controls · Computer system validation · Training and personnel The written specifications were inadequate.
2023-12-04
Health Canada
5 findingsEquipment and facility · Other quality system · Cleaning validation · Regulatory reporting and change control The maintenance of personnel records was inadequate. The job descriptions for personnel, the authority given to personnel, and/or the delegation of duties was inadequate and/or undocumented. The training of personnel before new or revised standard operating procedures were implemented was inadequate.
2023-12-04
Health Canada
5 findingsOther quality system · Regulatory reporting and change control · Cleaning validation · Equipment and facility The handling of standard operating procedures for good manufacturing practices was inadequate.
2023-12-04
Health Canada
5 findingsRegulatory reporting and change control · Equipment and facility · Cleaning validation · Other quality system The change control system was inadequate for ensuring changes are properly documented, evaluated, and/or approved.
2023-12-04
Health Canada
5 findingsRegulatory reporting and change control · Cleaning validation · Equipment and facility · Other quality system The change control system was inadequate for ensuring changes are properly documented, evaluated, and/or approved.
2023-12-04
Health Canada
5 findingsRegulatory reporting and change control · Other quality system · Cleaning validation · Equipment and facility The change control system was inadequate for ensuring changes are properly documented, evaluated, and/or approved.
2023-12-04
Health Canada
5 findingsOther quality system · Equipment and facility · Regulatory reporting and change control · Cleaning validation The handling of standard operating procedures for good manufacturing practices was inadequate.
2023-12-04
Health Canada
5 findingsEquipment and facility · Cleaning validation · Regulatory reporting and change control · Other quality system The preventative maintenance and repair of the equipment was inadequate.
2023-12-04
Health Canada
5 findingsEquipment and facility · Cleaning validation · Other quality system · Regulatory reporting and change control The preventative maintenance and repair of the equipment was inadequate.
2023-09-12
Health Canada
5 findingsEquipment and facility · Other quality system · Regulatory reporting and change control · Deviation, CAPA, and investigation · Computer system validation The job descriptions for personnel, the authority given to personnel, and/or the delegation of duties was inadequate and/or undocumented. The maintenance of personnel records was inadequate.
2023-07-04
Health Canada
5 findingsOther quality system · Equipment and facility · Regulatory reporting and change control · Complaint and recall handling · Training and personnel The handling of standard operating procedures for good manufacturing practices was inadequate.
2023-06-08
Health Canada
6 findingsTraining and personnel · Quality unit oversight · Equipment and facility · Other quality system · Deviation, CAPA, and investigation · Laboratory and QC controls The job descriptions for personnel, the authority given to personnel, and/or the delegation of duties was inadequate and/or undocumented.
2023-03-13
Health Canada
12 findingsLaboratory and QC controls · Equipment and facility · Other quality system · Computer system validation · Deviation, CAPA, and investigation · Material and supplier control · Quality unit oversight · Regulatory reporting and change control The quality control department did not undertake all of the required activities.
2022-11-29
Health Canada
4 findingsEquipment and facility · Laboratory and QC controls · Regulatory reporting and change control The availability, content and/or maintenance of the quality agreements between the supplier, fabricator, tester, packager, labeller, distributor, importer, and/or wholesaler was inadequate.
2022-11-24
Health Canada
7 findingsOther quality system · Regulatory reporting and change control · Complaint and recall handling · Equipment and facility · Deviation, CAPA, and investigation · Computer system validation The written self-inspection procedure was inadequate.
2022-11-03
Health Canada
3 findingsOther quality system · Complaint and recall handling The controls were inadequate for creating, modifying, reviewing, storing, and/or retrieving records.
2022-03-15
Health Canada
4 findingsComputer system validation · Quality unit oversight · Deviation, CAPA, and investigation · Labeling and packaging The calibration, inspection, and/or qualification of the equipment, including computerized systems, was inadequate.
2021-10-18
Health Canada
5 findingsLaboratory and QC controls · Training and personnel · Other quality system The creation, maintenance, processing, and/or review of laboratory data was inadequate.
2021-01-13
Health Canada
9 findingsOther quality system · Quality unit oversight · Equipment and facility · Laboratory and QC controls · Regulatory reporting and change control The handling of standard operating procedures for good manufacturing practices was inadequate. The system for reviewing, revising, and approving standard operating procedures was inadequate.
About this page
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.
What is included. As of 2026-09-03, only documents that have a detail page (at least 3 findings) are listed. The company may have more documents; the full set is available in Company lookup below.
Companies are grouped by a normalised key, not the displayed name — “… Limited” and “… Ltd.” count as the same company. Translation and classification are automated and may differ in nuance from the source; the basis for judgement is always the regulator's published document.
