1Equipment and facility
Evaluation of production processes, equipment, and/or materials was inadequate.
Inspection Record
Teva Canada Limited — Health Canada Inspection Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
2Other quality system
The recorded information or details were inadequate.
3Stability and storage
The temperature and/or humidity control was inadequate.
4Cleaning validation
The implementation, effectiveness, and/or validation of the cleaning procedures was inadequate for preventing unsanitary conditions.
5Equipment and facility
The design, location, and/or maintenance of the equipment was inadequate for allowing the equipment to serve its intended purpose
6Equipment and facility
The maintenance of the premises was inadequate.
About this record
Extracted automatically from the document of the Health Canada inspection on 2021-12-06. 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.
