1Deviation, CAPA, and investigation
Investigations into deviations, reports, and/or follow-up actions were inadequate.
Inspection Record
3DM Group (Division of 171840 Canada Inc.) — Health Canada Inspection Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
2Laboratory and QC controls
The quality control department did not approve, sign, and/or date the good manufacturing practices documents and/or the standard operating procedures.
3Material and supplier control
The handling of raw materials, products, or packaging materials in keeping with pre-approved written procedures or instructions was inadequate.
4Computer system validation
A preventative maintenance system had not been established for the equipment used in significant processing and/or testing operations The calibration, inspection, and/or qualification of the equipment, including computerized systems, was inadequate.
5Other quality system
The written self-inspection procedure was inadequate.
About this record
Extracted automatically from the document of the Health Canada inspection on 2026-08-11. The source is available at the link above.
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.
Translation and classification are automated and may differ in nuance from the source.
