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Sapron Beauty & Laser Spa

2365 - Maple Road NW Edmonton AB T6T 0Y3 · Personal Services

Official record from Alberta →

Inspection summary

Sapron Beauty & Laser Spa has been inspected 3 times by Alberta Health Services (Environmental Public Health) since October 26, 2023. The most recent inspection, on January 10, 2024, found no infractions.

1 of 3 inspections on record found no infractions at all. No inspections are on record from the past 12 months. All recorded findings relate to upkeep, equipment or paperwork rather than direct infection-control risks to clients.

What these findings mean

Health authorities word their findings differently, so we group them by what they mean for clients. In personal service settings like salons, spas and tattoo studios, higher-risk findings are the ones that could spread infection from one client to the next, through broken skin, blood or instruments that were not properly cleaned and sterilized.

  • Equipment and utensilsLower risk

    Instruments, chairs, tables and footbaths must be made of materials that can be cleaned, kept in good repair and stored so they stay clean. Single-use items such as nail files, buffers, razors and needles must be thrown away after each client.

    Recorded 7 times across 2 separate inspections, most recently on December 15, 2023. For example: Is reusable equipment disinfected properly?

  • Permits, records and postingLower risk

    Operating permits, client records, sterilization logs and required signage. Client records matter because they let health officials contact people if an infection is linked to the business.

    Recorded 3 times across 2 separate inspections, most recently on December 15, 2023. For example: Are facility-specific written procedures established to adequately describe safe and sanitary practices?

About this data

These results come from Alberta Health Services (Environmental Public Health), which inspects food premises and other public facilities in this area. We republish the authority's public disclosure data and refresh it regularly; the official record is the final word.

3 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?
      • -Written procedures were not available for this facility. Please ensure written procedures are developed for: Preparation of Skin, Post-Service Car and Client Care.
    • 20. Is reusable equipment disinfected properly?
      • - Pre-empt CS20 was being used to disinfect equipment but equipment was not being fully immersed in the high-level disinfectant during the disinfection process. - High level disinfectants are not being tested and verified daily using proper test strips. Ensure records are kept of: test dates, whether the solution passed/failed, when the disinfectant was changed and the worker’s initials who performed the activity.Ensure the high level disinfectant is tested daily using the test strips specified by the disinfectant manufacturer.
    • 25. Are the equipment manufacturer's instructions for use of specific equipment available and followed?
      • Last Inspection:-The manufacturer’s instructions for the Hydrafacial machine and the Microdermabrasion machine are not kept in an accessible place. Current Inspection:- Still no instructions for the microdermabrasion unit. Ensure all booklets from manufacturer's are available.
  3. Monitoring Inspection

    7 infractions

    • 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
      • -Written procedures were not available for this facility. Please ensure written procedures are developed for: Preparation of Skin, Post-Service Car and Client Care.
    • 10. Is cleansing and antisepsis of skin and mucous membrane performed in accordance to written procedures and are suitable products being used?
      • -An antiseptic product is not being applied prior to a service that will puncture the skin. Ensure an antiseptic product is used prior to PMU services.
    • 13. Is single-use or uncleanable equipment being used as intended (Critical)?
      • - Porous or uncleanable equipment is not being discarded after each use. There was an orange stick and a single use nail file soaking in disinfectant. Equipment classified as porous or uncleanable must be discarded after use in one personal service on one client.-Lancets, which are considered single use were being re-used. Ensure sharps are disposed of after each use.*Single use disposable lancets are available for purchase.
    • 17. Is reusable equipment cleaned properly (Critical)?
      • - Used equipment was not being adequately cleaned and dried prior to disinfection. Waxing tools, the tint bowl and applicator were stored unclean. Ensure equipment is: disassembled, cleaned to remove soil, and rinsed and dried prior to disinfection or sterilization.*It is strongly recommended that a single use mixing bowl and applicator are used for lash/brow tinting.
    • 20. Is reusable equipment disinfected properly?
      • - Pre-empt CS20 was being used to disinfect equipment but equipment was not being fully immersed in the high-level disinfectant during the disinfection process. Ensure equipment is fully immersed in solution.- High level disinfectants are not being tested and verified daily using proper test strips. Ensure records are kept of: test dates, whether the solution passed/failed, when the disinfectant was changed and the worker’s initials who performed the activity.Ensure the high level disinfectant is tested daily using the test strips specified by the disinfectant manufacturer.-Staff indicated that Barbicide is changed every 5 days. Manufacturer’s instructions indicate that it needs to be changed daily. Ensure that it is changed daily.-Alcohol was being used to disinfect wax tools; this is not an appropriate disinfectant. Ensure at minimum a low level disinfectant is used on waxing tools.
    • 21. Is equipment that is intended to be sterile maintained sterile at the point of use?
      • - Sterility assurance documentation was not available for all equipment purchased as sterile (microneedling cartridges). Ensure appropriate documentation is available for equipment that is purchased as sterile.
    • 25. Are the equipment manufacturer's instructions for use of specific equipment available and followed?
      • -The manufacturer’s instructions for the Hydrafacial machine and the Microdermabrasion machine are not kept in an accessible place. Please ensure that manufacturer’s instructions are available in an accessible location.

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