1Computer system validation
The calibration, inspection, and/or qualification of the equipment, including computerized systems, was inadequate.
Inspection Record
HYTN Cannabis Inc. — Health Canada Inspection Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
2Material and supplier control
The specifications for any packaging materials were incomplete or inadequate.
3Other quality system
The master formulas to control the manufacturing process were inadequate. Line clearance was not performed before starting new processing operations.
4Cleaning validation
The sanitation programs were not adequately designed to identify and/or reduce the risks of contamination. The sanitation program was inadequate in its cleaning procedures, frequency of cleaning, procedures for waste disposal, and/or pest control measures. The availability, implementation, and/or quality of the written sanitation program was inadequate.
5Stability and storage
The design of the drug stability study was inadequate and/or not justified with a documented rationale.
6Material and supplier control
The specifications for any packaging materials were incomplete or inadequate. The handling of raw materials, products, or packaging materials in keeping with pre-approved written procedures or instructions was inadequate.
7Other quality system
Critical production processes were not validated.
About this record
Extracted automatically from the document of the Health Canada inspection on 2025-07-14. 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.
