This report shall not be reproduced, unless in its entirety, without written approval from Kaycha Labs. This report is an Kaycha Labs certification. The results relate only to the material or product analyzed. Test results are confidential unless explicitly waived otherwise. Void after 1 year from test end date. Cannabinoid content of batch material may vary depending on sampling error. IC=In-control QC parameter, NC=Non-controlled QC parameter, ND=Not Detected, NA=Not Analyzed, ppm=Parts Per Million, ppb=Parts Per Billion. Limit of Detection (LoD) and Limit Of Quantitation (LoQ) are terms used to describe the smallest concentration that can be reliably measured by an analytical procedure. RPD=Reproducibility of two measurements. Action Levels are State determined thresholds for human safety for consumption and/or inhalation. The result >99% are variable based on uncertainty of measurement (UM) for the analyte. The UM error is available from the lab upon request.The "Decision Rule" for the pass/fail does not include the UM. The limits are based on F.S. Rule 64-4.310. Jorge Segredo Lab Director State License # CMTL-0002 ISO Accreditation # 97164 ___________________ Signature 07/08/2020 ___________________ Signed On 4131 SW 47th AVENUE SUITE 1408 DAVIE, FL, 33314, USA Kaycha Labs CBD/CBG Menthol Ice N/A Matrix: Derivative Certificate of Analysis Sample:DA00623006-017 Harvest/Lot ID: 003 Seed to Sale #N/A Batch Date :N/A Batch#: 17-061620 Sample Size Received: 60 ml gram Retail Product Size: 60 ml gram Ordered : 06/18/20 Sampled : 06/18/20 Completed: 07/08/20 Expires: 07/08/21 Sampling Method: SOP Client Method Jul 08, 2020 | Flower Child CBD 632 W. Gunnison Ave Grand Junction , CO, 81501, USA PASSED Page 1 of 4 PRODUCT IMAGE SAFETY RESULTS MISC. Pesticides PASSED Heavy Metals PASSED Microbials PASSED Mycotoxins PASSED Residuals Solvents PASSED Filth PASSED Water Activity NOT TESTED Moisture NOT TESTED Terpenes NOT TESTED CANNABINOID RESULTS Total THC 0.050% THC/Container :27.600 mg Total CBD 0.881% CBD/Container :486.312 mg Total Cannabinoids 1.311% Total Cannabinoids/Container :723.672 mg CBC CBGA CBG THCV D8-THC CBDV CBN CBDA CBD D9-THC THCA 0.011% ND 0.369% ND ND ND ND ND 0.881% 0.050% ND 0.110 mg/g ND 3.690 mg/g ND ND ND ND ND 8.810 mg/g 0.500 mg/g ND LOD 0.001 0.001 0.001 0.001 0.001 0.001 0.001 0.001 0.0001 0.0001 0.001 % % % % % % % % % % % Cannabinoid Profile Test Analyzed by Weight Extraction date : Extracted By : 450 2.6721g 06/24/20 03:06:01 574 Analysis Method -SOP.T.40.020, SOP.T.30.050 Reviewed On - 06/25/20 13:15:01 Analytical Batch -DA013402POT Instrument Used : DA-LC-003 Batch Date : 06/24/20 14:18:49 Reagent Dilution Consums. ID 061220.16 400 280670723 031820.R16 918C4-918J 062420.R03 914C4-914AK 062420.R02 929C6-929H 76262-590 Full spectrum cannabinoid analysis utilizing High Performance Liquid Chromatography with UV detection (HPLC-UV). (Method: SOP.T.30.050 for sample prep and Shimadzu High Sensitivity Method SOP.T.40.020 for analysis. LOQ for all cannabinoids is 1 mg/L). Filth PASSED Analyzed By Weight Extraction date LOD(ppm) Extracted By 457 1g NA NA Analysis Method -SOP.T.40.013 Batch Date : 06/23/20 10:22:10 Analytical Batch -DA013362FIL Reviewed On - 06/23/20 10:31:24 Instrument Used : Filth/Foreign Material Microscope This includes but is not limited to hair, insects, feces, packaging contaminants, and manufacturing waste and by-products. An SH-2B/T Stereo Microscope is use for inspection.
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This report shall not be reproduced, unless in its entirety, without written approval from Kaycha Labs. This report isan Kaycha Labs certification. The results relate only to the material or product analyzed. Test results areconfidential unless explicitly waived otherwise. Void after 1 year from test end date. Cannabinoid content of batchmaterial may vary depending on sampling error. IC=In-control QC parameter, NC=Non-controlled QC parameter,ND=Not Detected, NA=Not Analyzed, ppm=Parts Per Million, ppb=Parts Per Billion. Limit of Detection (LoD) andLimit Of Quantitation (LoQ) are terms used to describe the smallest concentration that can be reliably measured byan analytical procedure. RPD=Reproducibility of two measurements. Action Levels are State determined thresholdsfor human safety for consumption and/or inhalation. The result >99% are variable based on uncertainty ofmeasurement (UM) for the analyte. The UM error is available from the lab upon request.The "Decision Rule" for thepass/fail does not include the UM. The limits are based on F.S. Rule 64-4.310.
Jorge SegredoLab Director
State License # CMTL-0002ISO Accreditation # 97164 ___________________
Signature
07/08/2020
___________________Signed On
4131 SW 47th AVENUE SUITE 1408DAVIE, FL, 33314, USA
Kaycha LabsCBD/CBG Menthol Ice
N/AMatrix: Derivative
Certificateof Analysis
Sample:DA00623006-017Harvest/Lot ID: 003
Seed to Sale #N/ABatch Date :N/A
Batch#: 17-061620Sample Size Received: 60 ml gram
Retail Product Size: 60 ml gramOrdered : 06/18/20Sampled : 06/18/20
76262-590Full spectrum cannabinoid analysis utilizing High Performance Liquid Chromatography with UV detection (HPLC-UV). (Method: SOP.T.30.050 forsample prep and Shimadzu High Sensitivity Method SOP.T.40.020 for analysis. LOQ for all cannabinoids is 1 mg/L).
Filth PASSED
Analyzed By Weight Extraction date LOD(ppm) Extracted By457 1g NA NA
Analysis Method -SOP.T.40.013 Batch Date : 06/23/20 10:22:10Analytical Batch -DA013362FIL Reviewed On - 06/23/20 10:31:24Instrument Used : Filth/Foreign Material Microscope
This includes but is not limited to hair, insects, feces, packaging contaminants, and manufacturing wasteand by-products. An SH-2B/T Stereo Microscope is use for inspection.
This report shall not be reproduced, unless in its entirety, without written approval from Kaycha Labs. This report isan Kaycha Labs certification. The results relate only to the material or product analyzed. Test results areconfidential unless explicitly waived otherwise. Void after 1 year from test end date. Cannabinoid content of batchmaterial may vary depending on sampling error. IC=In-control QC parameter, NC=Non-controlled QC parameter,ND=Not Detected, NA=Not Analyzed, ppm=Parts Per Million, ppb=Parts Per Billion. Limit of Detection (LoD) andLimit Of Quantitation (LoQ) are terms used to describe the smallest concentration that can be reliably measured byan analytical procedure. RPD=Reproducibility of two measurements. Action Levels are State determined thresholdsfor human safety for consumption and/or inhalation. The result >99% are variable based on uncertainty ofmeasurement (UM) for the analyte. The UM error is available from the lab upon request.The "Decision Rule" for thepass/fail does not include the UM. The limits are based on F.S. Rule 64-4.310.
Jorge SegredoLab Director
State License # CMTL-0002ISO Accreditation # 97164 ___________________
Signature
07/08/2020
___________________Signed On
4131 SW 47th AVENUE SUITE 1408DAVIE, FL, 33314, USA
Pesticide screen is performed using LC-MS which can screen down to below single digit ppb concentrations forregulated Pesticides. Currently we analyze for 67 Pesticides. (Method: SOP.T.30.060 Sample Preparation forPesticides Analysis via LCMSMS and SOP.T40.065 Procedure for Pesticide Quantification Using LCMS). * VolatilePesticide screening is performed using GC-MS which can screen down to below single digit ppb concentrationsfor regulated Pesticides. Analytes marked with an asterisk were tested using GC-MS.
This report shall not be reproduced, unless in its entirety, without written approval from Kaycha Labs. This report isan Kaycha Labs certification. The results relate only to the material or product analyzed. Test results areconfidential unless explicitly waived otherwise. Void after 1 year from test end date. Cannabinoid content of batchmaterial may vary depending on sampling error. IC=In-control QC parameter, NC=Non-controlled QC parameter,ND=Not Detected, NA=Not Analyzed, ppm=Parts Per Million, ppb=Parts Per Billion. Limit of Detection (LoD) andLimit Of Quantitation (LoQ) are terms used to describe the smallest concentration that can be reliably measured byan analytical procedure. RPD=Reproducibility of two measurements. Action Levels are State determined thresholdsfor human safety for consumption and/or inhalation. The result >99% are variable based on uncertainty ofmeasurement (UM) for the analyte. The UM error is available from the lab upon request.The "Decision Rule" for thepass/fail does not include the UM. The limits are based on F.S. Rule 64-4.310.
Jorge SegredoLab Director
State License # CMTL-0002ISO Accreditation # 97164 ___________________
Signature
07/08/2020
___________________Signed On
4131 SW 47th AVENUE SUITE 1408DAVIE, FL, 33314, USA
Sample Size Received : 60 ml gramCompleted : 07/08/20Expires: 07/08/21Sample Method : SOP Client Method
Page 3 of 4
Residual Solvents PASSED
Solvent LOD Units ActionLevel(PPM)
Pass/Fail Result
1,1-DICHLOROETHENE 0.8 ppm 8 PASS ND
1,2-DICHLOROETHANE 0.2 ppm 2 PASS ND
2-PROPANOL 50 ppm 500 PASS ND
ACETONE 75 ppm 750 PASS ND
ACETONITRILE 6 ppm 60 PASS ND
BENZENE 0.1 ppm 1 PASS ND
BUTANES (N-BUTANE) 500 ppm 5000 PASS ND
CHLOROFORM 0.2 ppm 2 PASS ND
DICHLOROMETHANE 12.5 ppm 125 PASS ND
ETHANOL 500 ppm PASS ND
ETHYL ACETATE 40 ppm 400 PASS ND
ETHYL ETHER 50 ppm 500 PASS ND
ETHYLENE OXIDE 0.5 ppm 5 PASS ND
HEPTANE 500 ppm 5000 PASS ND
METHANOL 25 ppm 250 PASS ND
N-HEXANE 25 ppm 250 PASS ND
PENTANES (N-PENTANE) 75 ppm 750 PASS ND
PROPANE 500 ppm 5000 PASS ND
TOLUENE 15 ppm 150 PASS ND
TOTAL XYLENES 15 ppm 150 PASS ND
TRICHLOROETHYLENE 2.5 ppm 25 PASS ND
Residual Solvents PASSED
Analyzed by Weight Extraction date Extracted By850 0.0208g 06/24/20 03:06:47 850
Analysis Method -SOP.T.40.032Analytical Batch -DA013405SOL Reviewed On - 06/26/20 14:27:24Instrument Used : DA-GCMS-003Batch Date : 06/24/20 14:52:35
Reagent Dilution Consums. ID
1 H2017.07700279984161291-1
Residual solvents screening is performed using GC-MS which can detect belowsingle digit ppm concentrations. Currently we analyze for 21 Residualsolvents.(Method: SOP.T.30.032 Residual Solvents Analysis via GC-MS).
This report shall not be reproduced, unless in its entirety, without written approval from Kaycha Labs. This report isan Kaycha Labs certification. The results relate only to the material or product analyzed. Test results areconfidential unless explicitly waived otherwise. Void after 1 year from test end date. Cannabinoid content of batchmaterial may vary depending on sampling error. IC=In-control QC parameter, NC=Non-controlled QC parameter,ND=Not Detected, NA=Not Analyzed, ppm=Parts Per Million, ppb=Parts Per Billion. Limit of Detection (LoD) andLimit Of Quantitation (LoQ) are terms used to describe the smallest concentration that can be reliably measured byan analytical procedure. RPD=Reproducibility of two measurements. Action Levels are State determined thresholdsfor human safety for consumption and/or inhalation. The result >99% are variable based on uncertainty ofmeasurement (UM) for the analyte. The UM error is available from the lab upon request.The "Decision Rule" for thepass/fail does not include the UM. The limits are based on F.S. Rule 64-4.310.
Jorge SegredoLab Director
State License # CMTL-0002ISO Accreditation # 97164 ___________________
Signature
07/08/2020
___________________Signed On
4131 SW 47th AVENUE SUITE 1408DAVIE, FL, 33314, USA
Analysis Method -SOP.T.30.065, SOP.T.40.065Analytical Batch -DA013372MYC | Reviewed On - 07/01/20 10:42:07Instrument Used : DA-LCMS-001_DER (MYC)Batch Date : 06/23/20 11:47:25
Analyzed by Weight Extraction date Extracted By585 1g 06/23/20 04:06:15 585
Aflatoxins B1, B2, G1, G2, and Ochratoxins A testing using LC-MS. (Method: SOP.T.30.065 forSample Preparation and SOP.T40.065 Procedure for Mycotoxins Quantification Using LCMS. LOQ 1.0ppb). Aflatoxin B1, B2, G1, and G2 must individually be <20ug/Kg. Ochratoxins must be <20µg/Kg.
Microbials PASSED
Analyte ResultASPERGILLUS_FLAVUS not present in 1 gram.ASPERGILLUS_FUMIGATUS not present in 1 gram.ASPERGILLUS_NIGER not present in 1 gram.ASPERGILLUS_TERREUS not present in 1 gram.ESCHERICHIA_COLI_SHIGELLA_SPP not present in 1 gram.SALMONELLA_SPECIFIC_GENE not present in 1 gram.
Analysis Method -SOP.T.40.043 / SOP.T.40.045Analytical Batch -DA013342MIC | Reviewed On - 06/27/20 14:41:05Instrument Used : PathogenDX PCR_Array Scanner DA-111,PathogenDX PCR_DA-013Batch Date : 06/23/20 08:44:42
Analyzed by Weight Extraction date Extracted By513 1.0509g 06/23/20 12:06:55 1082
Microbiological testing for Fungal and Bacterial Identification via Polymerase Chain Reaction (PCR)method consisting of sample DNA amplified via tandem Polymerase Chain Reaction (PCR) as acrude lysate which avoids purification. (Method SOP.T.40.043) If a pathogenic Escherichia Coli,Salmonella, Aspergillus fumigatus, Aspergillus flavus, Aspergillus niger, or Aspergillus terreus isdetected in 1g of a sample, the sample fails the microbiological-impurity testing.
Analyzed by Weight Extraction date Extracted By457 0.2503g 06/23/20 12:06:43 1022
Analysis Method -SOP.T.40.050, SOP.T.30.052Analytical Batch -DA013358HEA | Reviewed On - 06/25/20 07:51:08Instrument Used : DA-ICPMS-002Batch Date : 06/23/20 09:48:39
Heavy Metals screening is performed using ICP-MS (Inductively Coupled Plasma – MassSpectrometer) which can screen down to below single digit ppb concentrations for regulated heavymetals using Method SOP.T.30.052 Sample Preparation for Heavy Metals Analysis via ICP-MS andSOP.T.40.050 Heavy Metals Analysis via ICP-MS.