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 # CMTL-0001 ISO Accreditation # 97164 ___________________ Signature 12/03/2020 ___________________ Signed On 2444 NE 1st Blvd Suite 700 Gainesville, FL, 32609, USA Kaycha Labs delta 8 N/A Matrix: Derivative Certificate of Analysis Sample:GA01124002-001 Harvest/Lot ID: 1776-6 Seed to Sale #N/A Batch Date :N/A Batch#: 6 Sample Size Received: 15 gram Retail Product Size: 1 Ordered : 11/19/20 Sampled : 11/19/20 Completed: 12/03/20 Expires: 12/03/21 Sampling Method: SOP Client Method Dec 03, 2020 | Pinnacle Hemp 2900 Davis Blvd Joplin, MO, 64804, US 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% Total CBD 0.000% Total Cannabinoids 74.289% CBDV CBDA CBGA CBG CBD THCV CBN D9-THC D8-THC CBC THCA ND ND ND ND ND ND ND ND 74.289 % ND ND ND ND ND ND ND ND ND ND 742.890 mg/g ND ND LOD 0.001 0.001 0.001 0.001 0.0001 0.001 0.001 0.0001 0.001 0.001 0.001 % % % % % % % % % % % Cannabinoid Profile Test Analyzed by Weight Extraction date : Extracted By : 508 0.0986g 11/24/20 06:11:48 2103 Analysis Method -SOP.T.40.020, SOP.T.30.050 Reviewed On - 11/25/20 16:26:03 Batch Date : 11/24/20 14:19:22 Analytical Batch -GA019203POT Instrument Used : GA-HPLC-001 2030C Plus (Carl) Running On : 11/25/20 09:43:01 Reagent Dilution Consums. ID 110520.27 40 280630187 111720.R10 VAV-09-1020 Lot# 947.077 111920.R01 6970145500298 190624060 16466-042 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 Extracted By 2103 12.0g 11/24/20 2103 Analyte LOD Result Filth and Foreign Material 0.1 ND Analysis Method -SOP.T.40.013 Batch Date : 11/24/20 13:30:58 Analytical Batch -GA019195FIL Reviewed On - 11/25/20 14:38:00 Instrument Used : GA-Filth/Foreign Material Microscope Running On : 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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N/A Matrix: Derivative Certificate Harvest/Lot ID: 1776-6 of ......(Method: SOP.T.30.050 for sample prep and Shimadzu High Sensitivity Method SOP.T.40.020 for analysis. LOQ for all
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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 # CMTL-0001ISO Accreditation # 97164 ___________________
Signature
12/03/2020
___________________Signed On
2444 NE 1st Blvd Suite 700Gainesville, FL, 32609, USA
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 PASSEDAnalyzed By Weight Extraction date Extracted By2103 12.0g 11/24/20 2103Analyte LOD ResultFilth and Foreign Material 0.1 NDAnalysis Method -SOP.T.40.013 Batch Date : 11/24/20 13:30:58Analytical Batch -GA019195FIL Reviewed On - 11/25/20 14:38:00Instrument Used : GA-Filth/Foreign Material MicroscopeRunning On :
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 # CMTL-0001ISO Accreditation # 97164 ___________________
Signature
12/03/2020
___________________Signed On
2444 NE 1st Blvd Suite 700Gainesville, FL, 32609, USA
Kaycha Labsdelta 8
N/AMatrix : Derivative
Certificate of Analysis PASSEDPinnacle Hemp
2900 Davis BlvdJoplin, MO, 64804, USTelephone: 8334367283Email: [email protected]
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.
Jeremy CampbellLab Director
State License # CMTL-0001ISO Accreditation # 97164 ___________________
Signature
12/03/2020
___________________Signed On
2444 NE 1st Blvd Suite 700Gainesville, FL, 32609, USA
Kaycha Labsdelta 8
N/AMatrix : Derivative
Certificate of Analysis PASSEDPinnacle Hemp
2900 Davis BlvdJoplin, MO, 64804, USTelephone: 8334367283Email: [email protected]
Analyzed by Weight Extraction date Extracted By508 .0270g 11/24/20 03:11:44 508
Analysis Method -SOP.T.40.032Analytical Batch -GA019197SOL Reviewed On - 11/25/20 16:00:23Instrument Used : GA-GCMS-001 Headspace SolventRunning On : 11/24/20 15:36:18Batch Date : 11/24/20 13:48:53
Reagent Dilution Consums. ID
24154107ach-20-1720
Residual solvents screening is performed using GC-MS which can detect belowsingle digit ppm concentrations. Currently we analyze for 21 Residualsolvents.(Method: SOP.T.40.032 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 # CMTL-0001ISO Accreditation # 97164 ___________________
Signature
12/03/2020
___________________Signed On
2444 NE 1st Blvd Suite 700Gainesville, FL, 32609, USA
Kaycha Labsdelta 8
N/AMatrix : Derivative
Certificate of Analysis PASSEDPinnacle Hemp
2900 Davis BlvdJoplin, MO, 64804, USTelephone: 8334367283Email: [email protected]
Analyte LOD 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.40.044Analytical Batch -GA019209MIC Batch Date : 11/24/20Instrument Used : GA-093 PathogenDx Scanner (MIC)Running On :
Analyzed by Weight Extraction date Extracted By1828 0.9816g 11/24/20 1748
Reagent Dilution Consums. ID110320.37 10 001001
001001002005
Microbiological testing for Fungal and Bacterial Identification via Polymerase Chain Reaction (PCR) methodconsisting of sample DNA amplified via tandem Polymerase Chain Reaction (PCR) as a crude lysate which avoidspurification. (Method SOP.T.40.043) If a pathogenic Escherichia Coli, Salmonella, Aspergillus fumigatus,Aspergillus flavus, Aspergillus niger, or Aspergillus terreus is detected in 1g of a sample, the sample fails themicrobiological-impurity testing.
Analysis Method -SOP.T.30.065, SOP.T.40.065Analytical Batch -GA019378MYC | Reviewed On - 12/03/20 10:22:39Instrument Used : GA-LCMS-001 MYCRunning On : 12/01/20 18:22:39Batch Date : 12/01/20 11:22:40
Analyzed by Weight Extraction date Extracted By1850 1.1085g 12/02/20 12:12:17 1850
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.
Analyzed by Weight Extraction date Extracted By650 0.5024g 11/24/20 06:11:57 2119
Analysis Method -SOP.T.40.050, SOP.T.30.052Analytical Batch -GA019182HEA | Reviewed On - 11/25/20 13:58:47Instrument Used : GA-ICPMS-001-DER (Ice Princess)Running On : 11/25/20 09:47:34Batch Date : 11/24/20 10:48:29
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.
PharmLabs San Diego Certificate of Analysis3421 Hancock St, Second Floor, San Diego, CA 92110 | License: C8-0000098-LIC ISO/IEC 17025:2017 Certification L17-427-1 | Accreditation #85368
Sample Cherry Pie Batch 11Sample ID SD210119-005 (40865) Matrix Distillate - NI (Other Cannabis Good)Tested for Pinnacle HempSampled - Received Jan 18, 2021 Reported Jan 20, 2021Analyses executed CAN+
ND Not DetectedN/A Not ApplicableNT Not ReportedLOD Limit of DetectionLOQ Limit of Quantification<LOQ Detected>ULOL Above upper limit of linearityCFU/g Colony Forming Units per 1 gramTNTC Too Numerous to Count
Accreditation #85368
Scan the QR code toverify authenticity.
Authorized Signature
Dr. Lia Prevedello, Laboratory DirectorWed, 20 Jan 2021 14:36:08 -0800
PharmLabs San Diego | 3421 Hancock St, Second Floor, San Diego, CA 92110 | 619.356.0898 | ISO/IEC 17025:2017 Certification L17-427-1*This report shall not be reproduced except in full, without the written approval of the lab. This report is for informational purposes only and should not be used to diagnose, treat orprevent any disease. Results are only for samples and batches indicated. Results are reported on an "as received" basis, unless indicated otherwise.
PharmLabs San Diego Certificate of Analysis3421 Hancock St, Second Floor, San Diego, CA 92110 | License: C8-0000098-LIC ISO/IEC 17025:2017 Certification L17-427-1 | Accreditation #85368
Sample GG#4 Batch 11Sample ID SD210119-006 (40866) Matrix Distillate - NI (Other Cannabis Good)Tested for Pinnacle HempSampled - Received Jan 18, 2021 Reported Jan 20, 2021Analyses executed CAN+
ND Not DetectedN/A Not ApplicableNT Not ReportedLOD Limit of DetectionLOQ Limit of Quantification<LOQ Detected>ULOL Above upper limit of linearityCFU/g Colony Forming Units per 1 gramTNTC Too Numerous to Count
Accreditation #85368
Scan the QR code toverify authenticity.
Authorized Signature
Dr. Lia Prevedello, Laboratory DirectorWed, 20 Jan 2021 14:36:08 -0800
PharmLabs San Diego | 3421 Hancock St, Second Floor, San Diego, CA 92110 | 619.356.0898 | ISO/IEC 17025:2017 Certification L17-427-1*This report shall not be reproduced except in full, without the written approval of the lab. This report is for informational purposes only and should not be used to diagnose, treat orprevent any disease. Results are only for samples and batches indicated. Results are reported on an "as received" basis, unless indicated otherwise.