Skip to content
Loading map…

Cherish Does

339 Scott St, Fort Frances ON P9A 1H1 · Infection Control Premises

2 inspections

  1. Follow-up

    0 infractions

  2. Required

    6 infractions

    • Operator demonstrates competence in the infection prevention and control practices relevant to the services offered at the personal service setting
    • Accurate client records are kept for skin invasive procedures
      • Ensure client records include the procedure that was performed, and the body part that the procedure was performed on
      • Ensure client records include the lot and expiry date of the pre-packaged sterile equipment used in the proced
      • Ensure client records indicate that the information about the procedure and potential risk was provided to the client, as well as any after-care instructions
    • Ink caps and ink handled appropriately
      • Bulk disposable ink caps cleaned and disinfected prior to use.
    • Sterilizers are being monitored appropriately
      • Autoclaves, chemical autoclaves and dry heat sterilizers must have their operation monitored routinely.
      • Three forms of monitoring is required to ensure sterilization- Physical, Chemical and Biological.
      • Spore strips are to be sent to an accredited laboratory for testing as defined by the Laboratory and Specimen Collection Centre Licensing Act.
      • Every instrument must have a temperature sensitive indicator which changes color if the packaged item was processed. Indicators must be specific type of sterilizer being used.
      • Biological monitoring must occur at least bi-weekly (every other week).
      • Three negative tests are required to demonstrate a new or back-up autoclave is functioning appropriately.
    • Sterilizers are being monitored appropriately
      • Autoclaves, chemical autoclaves and dry heat sterilizers must have their operation monitored routinely.
      • Three forms of monitoring is required to ensure sterilization- Physical, Chemical and Biological.
      • Spore strips are to be sent to an accredited laboratory for testing as defined by the Laboratory and Specimen Collection Centre Licensing Act.
      • Every instrument must have a temperature sensitive indicator which changes color if the packaged item was processed. Indicators must be specific type of sterilizer being used.
      • Biological monitoring must occur at least bi-weekly (every other week).
      • Three negative tests are required to demonstrate a new or back-up autoclave is functioning appropriately.
    • Accurate Records kept in regards to Sterilizer operation and maintenance
      • Sterilizer records and must include the name and type of sterilizer used
      • Sterilizer records must include the date and time when the sterilizer was used
      • Sterilizer records must include the equipment on which the sterilizer was used
      • Sterilizer records must include any preventative maintenance or repairs, and the results of any checks or tests that were completed
      • Sterilization records must include information about each load including temperature, duration, pressure, date, and the name of the individual responsible for monitoring the sterilization process
      • Sterilizer records must be held in a secure location for a minimum of one year and on file for five years.