Firm Record

Chief Medical Supplies Ltd findings history

96 findings from 8 inspection documents published by regulators. Each row below says what its date means.

Health Canada 2021-09-23 ~ 2025-06-16 8 documents 96 findings

Areas cited

Other quality systemLaboratory and QC controlsEquipment and facilityMaterial and supplier controlDeviation, CAPA, and investigationTraining and personnelStability and storageComputer system validationRegulatory reporting and change controlComplaint and recall handlingCleaning validationLabeling and packagingValidation and qualificationContamination controlQuality unit oversight

Published inspection documents

2025-06-16 Health Canada 11 findingsEquipment and facility · Other quality system · Complaint and recall handling · Laboratory and QC controls · Deviation, CAPA, and investigation · Training and personnel The preventative maintenance and repair of the equipment was inadequate. 2025-04-28 Health Canada 13 findingsOther quality system · Laboratory and QC controls · Stability and storage · Deviation, CAPA, and investigation · Training and personnel · Material and supplier control · Equipment and facility The monitoring procedures for microbial and/or environmental conditions were inadequate. 2024-03-04 Health Canada 7 findingsOther quality system · Equipment and facility · Laboratory and QC controls · Material and supplier control · Complaint and recall handling The traceability, legibility, documentation, formatting, and/or the accuracy of records was inadequate. 2024-02-20 Health Canada 12 findingsStability and storage · Equipment and facility · Laboratory and QC controls · Other quality system · Deviation, CAPA, and investigation · Computer system validation The stability program for a drug did not include a minimum of one batch of every strength of the drug for every year the drug was fabricated. 2023-04-11 Health Canada 19 findingsMaterial and supplier control · Other quality system · Stability and storage · Equipment and facility · Laboratory and QC controls · Training and personnel · Quality unit oversight · Deviation, CAPA, and investigation · Labeling and packaging · Computer system validation · Contamination control The sampling plan for raw materials was inadequate. Each container of a lot of raw materials was not tested to identify its contents with a specific, discriminating test. 2023-02-06 Health Canada 9 findingsOther quality system · Material and supplier control · Regulatory reporting and change control · Training and personnel · Computer system validation · Laboratory and QC controls The traceability, legibility, documentation, formatting, and/or the accuracy of records was inadequate. 2022-02-08 Health Canada 17 findingsEquipment and facility · Laboratory and QC controls · Material and supplier control · Validation and qualification · Other quality system · Stability and storage · Deviation, CAPA, and investigation · Cleaning validation · Computer system validation · Regulatory reporting and change control The establishment and/or the maintenance of a data governance plan was inadequate. 2021-09-23 Health Canada 8 findingsComplaint and recall handling · Other quality system · Labeling and packaging · Regulatory reporting and change control · Cleaning validation 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.

Full history of Chief Medical Supplies Ltd — including inspection classifications Browse by document Go to Findings search