Firm Record
Linde Canada Inc. findings history
52 findings from 13 inspection documents published by regulators. Each row below says what its date means.
Areas cited
Equipment and facilityOther quality systemQuality unit oversightDeviation, CAPA, and investigationComplaint and recall handlingComputer system validationRegulatory reporting and change controlCleaning validationLaboratory and QC controlsMaterial and supplier controlTraining and personnel
Published inspection documents
2026-02-18
Health Canada
3 findingsOther quality system · Deviation, CAPA, and investigation · Equipment and facility The implementation and/or the effectiveness of the sanitation program in preventing unsanitary conditions was inadequate.
2024-12-09
Health Canada
3 findingsEquipment and facility · Other quality system · Regulatory reporting and change control The validation of equipment or the planned maintenance of equipment was inadequate.
2024-11-15
Health Canada
4 findingsEquipment and facility · Complaint and recall handling · Laboratory and QC controls The preventative maintenance and repair of the equipment was inadequate.
2024-11-14
Health Canada
3 findingsOther quality system · Laboratory and QC controls · Equipment and facility The traceability, legibility, documentation, formatting, and/or the accuracy of records was inadequate.
2023-05-11
Health Canada
3 findingsMaterial and supplier control · Equipment and facility · Quality unit oversight The handling of raw materials, products, or packaging materials in keeping with pre-approved written procedures or instructions was inadequate.
2023-05-10
Health Canada
3 findingsEquipment and facility · Quality unit oversight · Material and supplier control The maintenance of records was inadequate.
2023-01-10
Health Canada
3 findingsCleaning validation · Deviation, CAPA, and investigation · Equipment and facility The sanitation program was inadequate in its cleaning procedures, frequency of cleaning, procedures for waste disposal, and/or pest control measures.
2022-12-14
Health Canada
3 findingsEquipment and facility · Quality unit oversight · Other quality system The design, location, and/or maintenance of the equipment was inadequate for allowing the equipment to serve its intended purpose
2022-11-29
Health Canada
3 findingsComplaint and recall handling · Cleaning validation · Computer system validation The assessment, recording, follow-up, and/or investigation of complaints and/or other information about potentially defective products was inadequate.
2022-11-25
Health Canada
6 findingsComplaint and recall handling · Quality unit oversight · Deviation, CAPA, and investigation · Computer system validation · Equipment and facility · Other quality system The written procedures for recalls were inadequate.
2022-11-09
Health Canada
6 findingsDeviation, CAPA, and investigation · Training and personnel · Other quality system · Quality unit oversight · Equipment and facility The deviation investigations to reconcile bulk product or printed packaging materials were inadequate.
2022-11-09
Health Canada
7 findingsQuality unit oversight · Equipment and facility · Regulatory reporting and change control · Other quality system · Complaint and recall handling · Deviation, CAPA, and investigation The annual product quality review procedure was inadequate.
2022-10-26
Health Canada
5 findingsOther quality system · Computer system validation · Quality unit oversight The written self-inspection procedure 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.
