Areas cited
Other quality systemEquipment and facilityMaterial and supplier controlDeviation, CAPA, and investigationTraining and personnelRegulatory reporting and change controlComplaint and recall handlingLaboratory and QC controlsStability and storage
Published inspection documents
2026-02-02
Health Canada
3 findingsOther quality system · Stability and storage · Equipment and facility The handling of standard operating procedures for good manufacturing practices was inadequate.
2025-04-30
Health Canada
3 findingsOther quality system · Regulatory reporting and change control · Equipment and facility The handling of standard operating procedures for good manufacturing practices was inadequate. The traceability, legibility, documentation, formatting, and/or the accuracy of records was inadequate. The recorded information or details were inadequate.
2022-03-22
Health Canada
5 findingsDeviation, CAPA, and investigation · Material and supplier control · Equipment and facility · Laboratory and QC controls · Other quality system Investigations into deviations, reports, and/or follow-up actions were inadequate.
2021-10-18
Health Canada
8 findingsComplaint and recall handling · Material and supplier control · Training and personnel · Other quality system · Deviation, CAPA, and investigation The quality control department's handling of complaints and/or information received about drug quality 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.
