Black Diamond Tattoo Club
102 - 9925 Biggs Avenue Fort McMurray AB T9H 4K3 · Personal Services
9 inspections
- Risk Management Inspection
0 infractions
- Monitoring Inspection
0 infractions
- Risk Management Inspection
0 infractions
- Risk Management Inspection
3 infractions
- 21. Is equipment that is intended to be sterile maintained sterile at the point of use?
- Equipment with inadequate monitoring was not sterile at the point of use.Corrective Actions:- Ensure all sterilized jewllery or equipment without sterility assurance documentation are removed from use.Only use pre-sterilized jewelry until Autoclave pass the qualification test cycle and all jewelry and equipment is re-sterilized.- Once all corrective actions have been taken with respect to the sterilization process, repackage and sterilize all peel pouches without previous sterility assurance.
- 23. If the facility sterilizes equipment, are all proper sterilization, verification, and documentation processes in place (Non-Critical)?
- - Load numbers were no longer labeled on sterilization pouches.Corrective Actions Required:- Label peel pouches with the appropriate load number. Ensure labels are either on the plastic side of the peel pouch, or if on the paper side, located outside of the seal.
- 26. Are cosmetic products appropriate for their intended use and being handled properly?
- Chemical containing spray bottles were noted without labels in the facility. Reportedly bottle contain Cavicide intermediate disinfectant.Label all the bottles containing chemicals to indicate their contents correctly.
- 21. Is equipment that is intended to be sterile maintained sterile at the point of use?
- Risk Management Inspection
5 infractions
- 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
- Written procedures were not completed. Facility specific written procedures were discussed onsite and AHS Templates for required procedures were provided to be completed and provide copies to the undersign via email.Post care procedures for Tattoo and piercing were available.
- 12. Are personal services workers at the facility maintaining client records and where applicable, sterility documentation corresponding to that client?
- Sterility assurance documentation was not recorded with clients for piercing services.Ensure all sterility assurance documentation for piercing services is recorded with client record for tracking. Record must be maintained for 2 years.
- 21. Is equipment that is intended to be sterile maintained sterile at the point of use?
- Equipment with inadequate monitoring was not sterile at the point of use.Corrective Actions:- Ensure all sterilized jewllery or equipment without sterility assurance documentation are removed from use.Only use pre-sterilized jewelry until Autoclave pass the qualification test cycle and all jewelry and equipment is re-sterilized.- Once all corrective actions have been taken with respect to the sterilization process, repackage and sterilize all peel pouches without previous sterility assurance.
- 23. If the facility sterilizes equipment, are all proper sterilization, verification, and documentation processes in place (Non-Critical)?
- - Load numbers were no longer labeled on sterilization pouches.Corrective Actions Required:- Label peel pouches with the appropriate load number. Ensure labels are either on the plastic side of the peel pouch, or if on the paper side, located outside of the seal.
- 26. Are cosmetic products appropriate for their intended use and being handled properly?
- Chemical containing spray bottles were noted without labels in the facility. Reportedly bottle contain Cavicide intermediate disinfectant.Label all the bottles containing chemicals to indicate their contents correctly.
- 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
- Risk Management Inspection
6 infractions
- 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
- Written procedures were not completed. Facility specific written procedures were discussed onsite and AHS Templates for required procedures were provided to be completed and provide copies to the undersign via email.Post care procedures for Tattoo and piercing were available.
- 12. Are personal services workers at the facility maintaining client records and where applicable, sterility documentation corresponding to that client?
- Sterility assurance documentation was not recorded with clients for piercing services.Ensure all sterility assurance documentation for piercing services is recorded with client record for tracking. Record must be maintained for 2 years.
- 21. Is equipment that is intended to be sterile maintained sterile at the point of use?
- Equipment with inadequate monitoring was not sterile at the point of use.Corrective Actions:- Ensure all sterilized jewllery or equipment without sterility assurance documentation are removed from use.Only use pre-sterilized jewelry until Autoclave pass the qualification test cycle and all jewelry and equipment is re-sterilized.- Once all corrective actions have been taken with respect to the sterilization process, repackage and sterilize all peel pouches without previous sterility assurance.
- 22. If the facility sterilizes equipment, are all proper sterilization, verification, and documentation processes in place (Critical)?
- 1-Manufacturer Instruction for Use (MIFU) for Autoclave was not available 2-Sterilization procedures were inadequate:- Load numbers were no longer labeled on sterilization pouches.- Physical parameters temperature and time were not monitored and documented. - Type 5 internal chemical indicator was not used for chemical monitoring.- Biological indicator (BI) was not used.- Qualification of the sterilizer was not performed. No previous record of qualification of sterilizer cycle was availableCorrective Actions Required:- Run a successful BI, type 5 chemical indicator, document sterilization temperature and exposure time.- According to the MIFU, ensure the chamber reaches the required temperature within required time.- Label peel pouches with the appropriate load number. Ensure labels are either on the plastic side of the peel pouch, or if on the paper side, located outside of the seal.
- 23. If the facility sterilizes equipment, are all proper sterilization, verification, and documentation processes in place (Non-Critical)?
- Packages were not labeled with load numbersQualification test results were not available.
- 26. Are cosmetic products appropriate for their intended use and being handled properly?
- Chemical containing spray bottles were noted without labels in the facility. Reportedly bottle contain Cavicide intermediate disinfectant.Label all the bottles containing chemicals to indicate their contents correctly.
- 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
- Risk Management Inspection
6 infractions
- 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
- Written procedures were not completed. Facility specific written procedures were discussed onsite and AHS Templates for required procedures were provided to be completed and provide copies to the undersign via email.Post care procedures for Tattoo and piercing were available.
- 12. Are personal services workers at the facility maintaining client records and where applicable, sterility documentation corresponding to that client?
- Sterility assurance documentation was not recorded with clients for piercing services.Ensure all sterility assurance documentation for piercing services is recorded with client record for tracking. Record must be maintained for 2 years.
- 21. Is equipment that is intended to be sterile maintained sterile at the point of use?
- Equipment with inadequate monitoring was not sterile at the point of use.Corrective Actions:- Ensure all sterilized jewllery or equipment without sterility assurance documentation are removed from use.Only use pre-sterilized jewelry until Autoclave pass the qualification test cycle and all jewelry and equipment is re-sterilized.- Once all corrective actions have been taken with respect to the sterilization process, repackage and sterilize all peel pouches without previous sterility assurance.
- 22. If the facility sterilizes equipment, are all proper sterilization, verification, and documentation processes in place (Critical)?
- 1-Manufacturer Instruction for Use (MIFU) for Autoclave was not available 2-Sterilization procedures were inadequate:- Load numbers were no longer labeled on sterilization pouches.- Physical parameters temperature and time were not monitored and documented. - Type 5 internal chemical indicator was not used for chemical monitoring.- Biological indicator (BI) was not used.- Qualification of the sterilizer was not performed. No previous record of qualification of sterilizer cycle was availableCorrective Actions Required:- Run a successful BI, type 5 chemical indicator, document sterilization temperature and exposure time.- According to the MIFU, ensure the chamber reaches the required temperature within required time.- Label peel pouches with the appropriate load number. Ensure labels are either on the plastic side of the peel pouch, or if on the paper side, located outside of the seal.
- 23. If the facility sterilizes equipment, are all proper sterilization, verification, and documentation processes in place (Non-Critical)?
- Packages were not labeled with load numbersQualification test results were not available.
- 26. Are cosmetic products appropriate for their intended use and being handled properly?
- Chemical containing spray bottles were noted without labels in the facility. Reportedly bottle contain Cavicide intermediate disinfectant.Label all the bottles containing chemicals to indicate their contents correctly.
- 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
- Monitoring Inspection
7 infractions
- 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
- Written procedures were not completed. Facility specific written procedures were discussed onsite and AHS Templates for required procedures were provided to be completed and provide copies to the undersign via email.Post care procedures for Tattoo and piercing were available.
- 12. Are personal services workers at the facility maintaining client records and where applicable, sterility documentation corresponding to that client?
- Sterility assurance documentation was not recorded with clients for piercing services.Ensure all sterility assurance documentation for piercing services is recorded with client record for tracking. Record must be maintained for 2 years.
- 21. Is equipment that is intended to be sterile maintained sterile at the point of use?
- Equipment with inadequate monitoring was not sterile at the point of use.Corrective Actions:- Ensure all sterilized jewllery or equipment without sterility assurance documentation are removed from use.Only use pre-sterilized jewelry until Autoclave pass the qualification test cycle and all jewelry and equipment is re-sterilized.- Once all corrective actions have been taken with respect to the sterilization process, repackage and sterilize all peel pouches without previous sterility assurance.
- 22. If the facility sterilizes equipment, are all proper sterilization, verification, and documentation processes in place (Critical)?
- 1-Manufacturer Instruction for Use (MIFU) for Autoclave was not available 2-Sterilization procedures were inadequate:- Load numbers were no longer labeled on sterilization pouches.- Physical parameters temperature and time were not monitored and documented. - Type 5 internal chemical indicator was not used for chemical monitoring.- Biological indicator (BI) was not used.- Qualification of the sterilizer was not performed. No previous record of qualification of sterilizer cycle was availableCorrective Actions Required:- Run a successful BI, type 5 chemical indicator, document sterilization temperature and exposure time.- According to the MIFU, ensure the chamber reaches the required temperature within required time.- Label peel pouches with the appropriate load number. Ensure labels are either on the plastic side of the peel pouch, or if on the paper side, located outside of the seal.
- 23. If the facility sterilizes equipment, are all proper sterilization, verification, and documentation processes in place (Non-Critical)?
- Packages were not labeled with load numbersQualification test results were not available.
- 25. Are the equipment manufacturer's instructions for use of specific equipment available and followed?
- MIFU for the Autoclave was not available.Ensure manual for the Autoclave is available/accessible.
- 26. Are cosmetic products appropriate for their intended use and being handled properly?
- Chemical containing spray bottles were noted without labels in the facility. Reportedly bottle contain Cavicide intermediate disinfectant.Label all the bottles containing chemicals to indicate their contents correctly.
- 03. Are facility-specific written procedures established to adequately describe safe and sanitary practices?
- Demand Inspection
0 infractions