1Training and personnel
The job descriptions for personnel, the authority given to personnel, and/or the delegation of duties was inadequate and/or undocumented.
Inspection Record
G Production Inc. — Health Canada Inspection Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
2Cleaning validation
The sanitation programs were not adequately designed to identify and/or reduce the risks of contamination. The implementation, effectiveness, and/or validation of the cleaning procedures was inadequate for preventing unsanitary conditions.
3Other quality system
The receipt, preparation, and/or handling of reagents and culture media was inadequate.
4Laboratory and QC controls
The creation, maintenance, processing, and/or review of laboratory data was inadequate.
5Material and supplier control
Printed packaging materials were not stored in an area with restricted access. Packaging operations were not performed in keeping with the written operating procedures or specifications.
6Equipment and facility
The maintenance and/or monitoring of the ventilation system's air quality was inadequate.
About this record
Extracted automatically from the document of the Health Canada inspection on 2025-06-09. 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.
