Areas cited
Other quality systemEquipment and facilityAseptic processing and sterility assuranceMaterial and supplier controlDeviation, CAPA, and investigationLaboratory and QC controlsStability and storageComputer system validationTraining and personnelRegulatory reporting and change controlValidation and qualificationCleaning validationContamination control
Published inspection documents
2025-11-19
Health Canada
17 findingsEquipment and facility · Computer system validation · Validation and qualification · Other quality system · Aseptic processing and sterility assurance · Deviation, CAPA, and investigation · Material and supplier control · Laboratory and QC controls · Stability and storage Evaluation of production processes, equipment, and/or materials was inadequate.
2025-11-19
Health Canada
3 findingsOther quality system · Laboratory and QC controls · Equipment and facility The recorded information or details were inadequate.
2023-11-06
Health Canada
10 findingsAseptic processing and sterility assurance · Other quality system · Material and supplier control · Regulatory reporting and change control · Equipment and facility · Deviation, CAPA, and investigation The validation of aseptic processing was inadequate.
2022-10-18
Health Canada
14 findingsMaterial and supplier control · Aseptic processing and sterility assurance · Other quality system · Equipment and facility · Computer system validation · Stability and storage · Cleaning validation · Deviation, CAPA, and investigation The premises and/or the manufacturing process were inadequate for minimizing contamination of the drugs and/or materials during fabrication and/or packaging.
2021-10-12
Health Canada
18 findingsAseptic processing and sterility assurance · Laboratory and QC controls · Contamination control · Training and personnel · Stability and storage · Deviation, CAPA, and investigation · Other quality system · Equipment and facility · Material and supplier control The validation of aseptic processing 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.
