Areas cited
Other quality systemValidation and qualificationEquipment and facilityDeviation, CAPA, and investigationComputer system validationTraining and personnelComplaint and recall handlingLaboratory and QC controlsStability and storageLabeling and packaging
Published inspection documents
2023-10-03
Health Canada
10 findingsComplaint and recall handling · Equipment and facility · Deviation, CAPA, and investigation · Validation and qualification · Other quality system · Computer system validation · Training and personnel · Laboratory and QC controls The written procedures for recalls were inadequate.
2022-12-12
Health Canada
3 findingsOther quality system · Equipment and facility · Computer system validation The traceability, legibility, documentation, formatting, and/or the accuracy of records was inadequate. The recorded information or details were inadequate. The receipt, preparation, and/or handling of reagents and culture media was inadequate.
2021-05-10
Health Canada
7 findingsLabeling and packaging · Validation and qualification · Stability and storage · Other quality system · Deviation, CAPA, and investigation The importer did not ensure that the foreign sites use to fabricate, package/label, or test drug products met the requirements described in Guidance on Evidence to Demonstrate Drug GMP Compliance of Foreign Sites (GUI-0080).
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.
