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. Jeremy Campbell Lab Director State License # n/a ISO Accreditation # 97164 ___________________ Signature 05/25/2020 ___________________ Signed On 2444 NE 1st Blvd Suite 700 Kaycha Labs GOOD VIBES ISOLATE N/A Matrix: Derivative Certificate of Analysis Sample:GA00511001-002 Harvest/Lot ID: N/A Seed to Sale #N/A Batch Date :N/A Batch#: 2019008205 Sample Size Received: 110 gram Retail Product Size: 1 Ordered : 05/07/20 Sampled : 05/07/20 Completed: 05/25/20 Expires: 05/25/21 Sampling Method: SOP Client Method May 25, 2020 | pure science lab 6574 n state road 7 coconut creek florida, usa 33073 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 0.000% THC/Container :0.000 mg Total CBD 93.239% CBD/Container :932.391 mg Total Cannabinoids 93.239% Total Cannabinoids/Container :932.391 mg CBC CBGA CBG THCV D8-THC CBDV CBN CBDA CBD D9-THC THCA ND ND ND ND ND ND ND ND 93.239 % ND ND ND ND ND ND ND ND ND ND 932.390 mg/g ND 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 : 508 0.1017g 05/19/20 09:05:47 972 Analysis Method -SOP.T.40.020, SOP.T.30.050 Reviewed On - 05/25/20 21:17:56 Analytical Batch -GA012520POT Instrument Used : GA-HPLC-001 2030C Plus Batch Date : 05/19/20 09:43:19 Reagent Dilution Consums. ID 051820.R11 400 280678841 051820.R08 VAV-09-1020 Lot# 947.077 042720.02 6970145500298 190624060 VAV-09-1020 (947.077) / ALK-09-1412 (9291.179) 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 972 NA 05/13/20 972 Analysis Method -SOP.T.40.013 Batch Date : 05/13/20 10:24:13 Analytical Batch -GA012389FIL Reviewed On - 05/13/20 10:24:44 Instrument Used : GA-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.
Jeremy CampbellLab Director
State License # n/aISO Accreditation # 97164 ___________________
Full 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 By972 NA 05/13/20 972
Analysis Method -SOP.T.40.013 Batch Date : 05/13/20 10:24:13Analytical Batch -GA012389FIL Reviewed On - 05/13/20 10:24:44Instrument Used : GA-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.
Jeremy CampbellLab Director
State License # n/aISO Accreditation # 97164 ___________________
Signature
05/25/2020
___________________Signed On
2444 NE 1st Blvd Suite 700
Kaycha LabsGOOD VIBES ISOLATE
N/AMatrix : Derivative
Certificate of Analysis PASSEDpure science lab
6574 n state road 7 coconut creekflorida, usa 33073Telephone: 9544150942Email: [email protected]
Pesticide screen is performed using LC-MS which can screen down to below single digit ppb concentrationsfor regulated Pesticides. Currently we analyze for 67 Pesticides. (Method: SOP.T.30.060 Sample Preparationfor Pesticides Analysis via LCMSMS and SOP.T40.065 Procedure for Pesticide Quantification Using LCMS). *Volatile Pesticide screening is performed using GC-MS which can screen down to below single digit ppbconcentrations for 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.
Jeremy CampbellLab Director
State License # n/aISO Accreditation # 97164 ___________________
Signature
05/25/2020
___________________Signed On
2444 NE 1st Blvd Suite 700
Kaycha LabsGOOD VIBES ISOLATE
N/AMatrix : Derivative
Certificate of Analysis PASSEDpure science lab
6574 n state road 7 coconut creekflorida, usa 33073Telephone: 9544150942Email: [email protected]
Analyzed by Weight Extraction date Extracted By508 0.0264g 05/12/20 01:05:55 972
Analysis Method -SOP.T.40.032Analytical Batch -GA012366SOL Reviewed On - 05/18/20 10:41:46Instrument Used : GA-GCMS-001 Headspace SolventBatch Date : 05/12/20 13:45:46
Reagent Dilution Consums. ID
24154107164282-100279984
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.
Jeremy CampbellLab Director
State License # n/aISO Accreditation # 97164 ___________________
Signature
05/25/2020
___________________Signed On
2444 NE 1st Blvd Suite 700
Kaycha LabsGOOD VIBES ISOLATE
N/AMatrix : Derivative
Certificate of Analysis PASSEDpure science lab
6574 n state road 7 coconut creekflorida, usa 33073Telephone: 9544150942Email: [email protected]
Analysis Method -SOP.T.30.065, SOP.T.40.065Analytical Batch -GA012343 | Reviewed On - 05/15/20 17:12:46Instrument Used : DA-LCMS-002Batch Date : 05/12/20 09:07:22
Analyzed by Weight Extraction date Extracted By795 1.0018g 05/12/20 09:05:34 635
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 -GA012376MIC | Reviewed On - 05/18/20 10:41:28Instrument Used : GA-093 PathogenDx ScannerBatch Date : 05/13/20 08:48:33
Analyzed by Weight Extraction date Extracted By935 1.0162g 05/13/20 10:05:27 935
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 By1541 0.4923g 05/14/20 10:05:21 1541
Analysis Method -SOP.T.40.050, SOP.T.30.052Analytical Batch -GA012395HEA | Reviewed On - 05/18/20 10:41:35Instrument Used : GA-ICPMS-001-DERBatch Date : 05/13/20 14:40:29
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.