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Elite Beauty Spa / Elite Beauty Medi Spa

5 - 9228 144 Avenue NW Edmonton AB T5E 6A3 · Personal Services

6 inspections

  1. Risk Management Inspection

    0 infractions

  2. Risk Management Inspection

    3 infractions

    • 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
      • Facility-specific written procedures were not available at the time of inspection.Written procedures for antiseptic application are required for the following services: -microneedling-mole/skin tag removalWritten procedures for post-service care are required for the following services: -microneedling-mole/skin tag removal
    • 06. Do operators and personal services workers comply with the Personal Services Regulation and Standards and do they have the skills and knowledge to perform their duties in a safe and sanitary manner?
      • The manufacturer's instructions for use (MIFU) was available for the fibroblast plasma pen used, but it could not be confirmed if this particular model had a medical device license number issued by Health Canada. For plasma pen use, it must have the manufacturer’s instructions and medical device license number issued by Health Canada. Provide this office with the medical device license number issued by Health Canada or discontinue use of this particular model.
    • 25. Are the equipment manufacturer's instructions for use of specific equipment available and followed?
      • The manufacturer's instructions for use (MIFU) was not available for 1 energy-emitting equipment available on-site. The MIFU must be kept in an accessible place for reference by a personal services worker at all times. Obtain the MIFU for all energy-emitting equipment and provide this office with a copy. Ensure it is kept in an accessible place as required.
  3. Risk Management Inspection

    3 infractions

    • 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
      • Written procedures for antiseptic application are required for the following services: -microneedling-mole/skin tag removal
    • 06. Do operators and personal services workers comply with the Personal Services Regulation and Standards and do they have the skills and knowledge to perform their duties in a safe and sanitary manner?
      • The manufacturer's instructions for use (MIFU) was available for the fibroblast plasma pen used, but it could not be confirmed if this particular model had a medical device license number issued by Health Canada. For plasma pen use, it must have the manufacturer’s instructions and medical device license number issued by Health Canada. Provide this office with the medical device license number issued by Health Canada or discontinue use of this particular model.
    • 25. Are the equipment manufacturer's instructions for use of specific equipment available and followed?
      • The manufacturer's instructions for use (MIFU) was not available for 1 energy-emitting equipment available on-site. The MIFU must be kept in an accessible place for reference by a personal services worker at all times. Obtain the MIFU for all energy-emitting equipment and provide this office with a copy. Ensure it is kept in an accessible place as required.
  4. Risk Management Inspection

    2 infractions

    • 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
      • Written procedures for antiseptic application are required for the following services: -microneedling-mole/skin tag removal
    • 06. Do operators and personal services workers comply with the Personal Services Regulation and Standards and do they have the skills and knowledge to perform their duties in a safe and sanitary manner?
      • The manufacturer's instructions for use (MIFU) was available for the fibroblast plasma pen used, but it could not be confirmed if this particular model had a medical device license number issued by Health Canada. For plasma pen use, it must have the manufacturer’s instructions and medical device license number issued by Health Canada. Provide this office with the medical device license number issued by Health Canada or discontinue use of this particular model.
  5. Monitoring Inspection

    7 infractions

    • 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
      • Written procedure for accidental skin cuts or punctures was provided to the operator at the time of inspection.
    • 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
      • Facility-specific written procedures were not available at the time of inspection.Written procedures for cleansing skin are required for the following services: -dermal planing-microneedling-mole/skin tag removalWritten procedures for antiseptic application are required for the following services: -microneedling-mole/skin tag removalWritten procedures for post-service care are required for the following services: -microneedling-mole/skin tag removalWritten procedure for handwashing and equipment reprocessing sink decontamination is required.
    • 06. Do operators and personal services workers comply with the Personal Services Regulation and Standards and do they have the skills and knowledge to perform their duties in a safe and sanitary manner?
      • The manufacturer's instructions for use (MIFU) was available for the fibroblast plasma pen used, but it could not be confirmed if this particular model had a medical device license number issued by Health Canada. For plasma pen use, it must have the manufacturer’s instructions and medical device license number issued by Health Canada. Provide this office with the medical device license number issued by Health Canada or discontinue use of this particular model.
    • 06. Do operators and personal services workers comply with the Personal Services Regulation and Standards and do they have the skills and knowledge to perform their duties in a safe and sanitary manner?
      • pH test strips were being used to test cavicide. Re-iterated following manufacturer's instructions.High-level disinfectant logs were being maintained for cavicide. Re-iterated that cavicide disinfectant is an intermediate-level disinfectant and this procedure is not required.
    • 21. Is equipment that is intended to be sterile maintained sterile at the point of use?
      • Expired critical instruments were discarded at the time of inspection.Critical instruments that did not have sterility assurance information were discarded at the time of inspection.
    • 25. Are the equipment manufacturer's instructions for use of specific equipment available and followed?
      • The manufacturer's instructions for use (MIFU) was not available for all of the energy-emitting equipment available on-site. The MIFU must be kept in an accessible place for reference by a personal services worker at all times. Obtain the MIFU for all energy-emitting equipment and provide this office with a copy. Ensure it is kept in an accessible place as required.
    • 26. Are cosmetic products appropriate for their intended use and being handled properly?
      • Zena cosmetic products that were missing labelling information were removed from the facility at the time of inspection. Re-iterated proper labelling requirements.
  6. Risk Management Inspection

    3 infractions

    • 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
      • Facility-specific written procedures were not available at the time of inspection.Written procedures for cleansing skin are required for the following services: -dermal planing-microneedling-mole/skin tag removalWritten procedures for antiseptic application are required for the following services: -microneedling-mole/skin tag removalWritten procedures for post-service care are required for the following services: -microneedling-mole/skin tag removalWritten procedure for handwashing and equipment reprocessing sink decontamination is required.
    • 06. Do operators and personal services workers comply with the Personal Services Regulation and Standards and do they have the skills and knowledge to perform their duties in a safe and sanitary manner?
      • The manufacturer's instructions for use (MIFU) was available for the fibroblast plasma pen used, but it could not be confirmed if this particular model had a medical device license number issued by Health Canada. For plasma pen use, it must have the manufacturer’s instructions and medical device license number issued by Health Canada. Provide this office with the medical device license number issued by Health Canada or discontinue use of this particular model.
    • 25. Are the equipment manufacturer's instructions for use of specific equipment available and followed?
      • The manufacturer's instructions for use (MIFU) was not available for 1 energy-emitting equipment available on-site. The MIFU must be kept in an accessible place for reference by a personal services worker at all times. Obtain the MIFU for all energy-emitting equipment and provide this office with a copy. Ensure it is kept in an accessible place as required.