HomeMy WebLinkAbout#5253_2021_0630_TLH_FINAL
September 3, 2021
5253
Ms. Regina Danison
RDU Airport Authority
P.O. Box 80001
RDU Airport, NC 27623
Subject: North Carolina Wastewater/Groundwater Laboratory Certification (NC WW/GW
LC) Maintenance Inspection
Dear Ms. Danison:
Enclosed is a report for the inspection performed on June 30, 2021 by Thomas Halvosa. I
apologize for the delay in getting this report to you. Where Finding(s) are cited in this report,
a response is required. Within thirty days, please supply this office with a written item for item
description of how these Finding(s) were corrected. Please describe the steps taken to prevent
recurrence and include an implementation date for each corrective action. If the Finding(s) cited
in the enclosed report are not corrected, enforcement actions may be recommended. For
Certification maintenance, your laboratory must continue to carry out the requirements set forth
in 15A NCAC 2H .0800.
A copy of the laboratory’s Certified Parameter List at the time of the audit is attached. This list will
reflect any changes made during the audit. Copies of the checklists completed during the
inspection may be requested from this office. Thank you for your cooperation during the
inspection. If you have questions or need additional information, please contact me at (919) 733-
3908 Ext. 259.
Sincerely,
Beth Swanson
Technical Assistance & Compliance Specialist
Division of Water Resources
Attachment
cc: Todd Crawford, Thomas Halvosa, File #5253
On-Site Inspection Report
LABORATORY NAME: RDU Airport Authority
NC GENERAL PERMIT #: NCS000588
ADDRESS: 1000 Trade Drive
RDU Airport, NC 27623
CERTIFICATE #: 5253
DATE OF INSPECTION: June 30, 2021
TYPE OF INSPECTION: Field Municipal Maintenance
AUDITOR: Tom Halvosa
LOCAL PERSON CONTACTED:
Regina Danison
I. INTRODUCTION:
This laboratory was inspected by a representative of the North Carolina Wastewater/Groundwater
Laboratory Certification Branch (NC WW/GW LCB) to verify its compliance with the requirements of 15A
NCAC 02H .0800 for the analysis of compliance monitoring samples.
II. GENERAL COMMENTS:
The facility is neat and well organized and has all the equipment necessary to perform the analyses.
Staff was forthcoming and responded well to suggestions from the auditor.
All required Proficiency Testing (PT) Samples have been analyzed and the laboratory has fulfilled its PT
requirements for the 2021 PT Calendar Year.
Contracted analyses are performed by Environmental Conservation Laboratories, Inc. - Cary (Certification #
591).
The Approved Procedure documents for the analysis of the facility’s currently certified Field Parameters
were provided at the time of the inspection.
The laboratory submitted their Standard Operating Procedure (SOP) documents in advance of the
inspection. These documents were reviewed and deemed acceptable.
The laboratory is reminded that any time changes are made to laboratory procedures, the laboratory
must update the QA/SOP document(s) and inform relevant staff. Any changes made in response to the
pre-audit review or to Findings, Recommendations or Comments listed in this report must be
incorporated to insure the method is being performed as stated, references to methods are accurate,
and the QA and/or SOP document(s) is in agreement with each approved practice, test, analysis,
measurement, monitoring procedure or regulatory requirement being used in the laboratory. In some
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instances, the laboratory may need to create an SOP to document how new functions or policies will be
implemented.
The laboratory is also reminded that SOPs are required to be reviewed at least every two years and are
intended to describe procedures exactly as they are to be performed. Use of the word “should” is not
appropriate when describing requirements (e.g., Quality Control (QC) frequency, acceptance criteria, etc.).
Evaluate all SOPs for the proper use of the word “should”.
III. FINDINGS, REQUIREMENTS, COMMENTS AND RECOMMENDATIONS:
Documentation
Comment: The laboratory benchsheet for Dissolved Oxygen (DO) describes the post-analysis
calibration verification as a Post-Sample/End-of-day Buffer check. It is recommended that the
laboratory rename this the Post-Analysis Calibration Verification.
A. Finding: The laboratory benchsheets for DO and pH are lacking required documentation:
the proper units of measure.
Requirement: All laboratories shall use printable laboratory benchsheets. Certified Data
shall be traceable to the associated sample analyses and shall consist of: proper units of
measure. Each item shall be recorded each time samples are analyzed. Analyses shall
conform to methodologies found in Subparagraph (a)(1) of this Rule. Ref: 15A NCAC 02H
.0805 (g) (L).
Comment: The DO benchsheet is missing % for the Drift Check result and the pH
benchsheet is missing Standard Units (S.U.) for all results.
B. Finding: The laboratory benchsheets for DO, pH and Temperature are lacking required
documentation: the method or Standard Operating Procedure.
Requirement: All laboratories shall use printable laboratory benchsheets. Certified Data
shall be traceable to the associated sample analyses and shall consist of: the method or
Standard Operating Procedure. Each item shall be recorded each time samples are
analyzed. Analyses shall conform to methodologies found in Subparagraph (a)(1) of this
Rule. Ref: 15A NCAC 02H .0805 (g) (A).
C. Finding: The laboratory is not documenting traceability information for purchased materials,
reagents and standards.
Requirement: 15A NCAC 02H .0805 (a)(7)(K) and (g)(7) requires laboratories to have a
documented system of traceability for the purchase, preparation, and use of all chemicals,
reagents, standards, and consumables. That system must include documentation of the
following information: Date received, Date Opened (in use), Vendor, Lot Number, and
Expiration Date (where specified). A system (e.g., traceable identifiers) must be in place that
links standard/reagent preparation information to analytical batches in which the solutions
are used. Documentation of solution preparation must include the analyst’s initials, date of
preparation, the volume or weight of standard(s) used, the solvent and final volume of the
solution. This information as well as the vendor and/or manufacturer, lot number, and
expiration date must be retained for primary standards, chemicals, reagents, and materials
used for a period of five years. Consumable materials such as pH buffers, lots of pre-made
standards and/or media, solids and bacteria filters, etc. are included in this requirement.
Ref: NC WW/GW LCB Policy.
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Comment: The laboratory was provided with an example receipt log to use for documenting
traceability information for purchased materials, reagents and standards.
D. Finding: Error corrections are not properly performed.
Requirement: All documentation errors shall be corrected by drawing a single line through
the error so that the original entry remains legible. Entries shall not be obliterated by
erasures or markings. Wite-Out®, correction tape, or similar products designed to obliterate
documentation are not to be used; instead the correction shall be written adjacent to the
error. The correction shall be initialed by the responsible individual and the date of change
documented. Ref: 15A NCAC 02H .0805 (g) (1).
Comment: The June 5, 2020 PT had an incorrect error correction for the Sample ID. The
March 16, 2021 DO benchsheet had an incorrect error correction for the Pre-Sample
Calibration value. In both cases, the corrected result was written over the original result and
did not have an initial or date.
E. Finding: The pH laboratory benchsheet is lacking required documentation: value obtained
for the check standard buffer.
Requirement: Laboratory procedures shall comply with Subparagraph (a)(1) of this Rule.
Ref: 15A NCAC 02H .0805 (g) (4).
Requirement: The following must be documented in indelible ink whenever sample analysis
is performed. Value obtained for the check standard buffer. Ref: NC WW/GW LCB Approved
Procedure for the Analysis of pH.
Comment: The laboratory writes a check mark for the check standard buffer result instead
of the actual value obtained.
Proficiency Testing
F. Finding: Additional QC beyond what is routine for Compliance Samples is being analyzed
with PT Samples.
Requirement: Laboratories are required to analyze an appropriate PT Sample by each
parameter method on the laboratory’s CPL. The same PT Sample may be analyzed by one
or more methods. Laboratories shall conduct the analyses in accordance with their routine
testing, calibration and reporting procedures, unless otherwise specified in the instructions
supplied by the Accredited PT Sample Provider. This means that they are to be logged in
and analyzed using the same staff, sample tracking systems, standard operating procedures
including the same equipment, reagents, calibration techniques, analytical methods,
preparatory techniques (e.g., digestions, distillations and extractions) and the same quality
control acceptance criteria. PT Samples shall not be analyzed with additional quality control.
They are not to be replicated beyond what is routine for Compliance Sample analysis.
Although, it may be routine to spike Compliance Samples, it is neither required, nor
recommended, for PT Samples. PT sample results from multiple analyses (when this is the
routine procedure) must be calculated in the same manner as routine Compliance Samples.
Ref: Proficiency Testing Requirements, February 19, 2020, Revision 5, Section 3.6.
Comment: The laboratory analyzes the previous years’ PT as a known standard.
Laboratories must not analyze additional standards with known concentrations along with
PT Samples with unknown concentrations, as this is not the routine testing protocol for
Compliance Samples. This is not to say that they cannot be used for troubleshooting
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purposes before analyzing a remedial PT Sample. This would be considered part of the
corrective action plan.
G.Finding: PT Samples are not being analyzed in the same manner as routine Compliance
Samples.
Requirement: Laboratories are required to analyze an appropriate PT Sample by each
parameter method on the laboratory’s CPL. The same PT Sample may be analyzed by one
or more methods. Laboratories shall conduct the analyses in accordance with their routine
testing, calibration and reporting procedures, unless otherwise specified in the instructions
supplied by the Accredited PT Sample Provider. This means that they are to be logged in
and analyzed using the same staff, sample tracking systems, standard operating procedures
including the same equipment, reagents, calibration techniques, analytical methods,
preparatory techniques (e.g., digestions, distillations and extractions) and the same quality
control acceptance criteria. PT Samples shall not be analyzed with additional quality control.
They are not to be replicated beyond what is routine for Compliance Sample analysis.
Although, it may be routine to spike Compliance Samples, it is neither required, nor
recommended, for PT Samples. PT sample results from multiple analyses (when this is the
routine procedure) must be calculated in the same manner as routine Compliance Samples.
Ref: Proficiency Testing Requirements, February 19, 2020, Revision 5, Section 3.6.
Comment: The laboratory analyzes the PT Sample in duplicate and reports one result. The
laboratory does not analyze Compliance Samples in duplicate.
Dissolved Oxygen – Standard Methods, 4500 O G-2011 (Aqueous)
H.Finding: The laboratory does not take corrective action when the Post-Analysis Calibration
Verification is outside of acceptable limits.
Requirement: If quality control results fall outside established limits or indicate an analytical
problem, the laboratory shall identify the Root Cause of the failure. The problem shall be
resolved through corrective action, the corrective action process documented, and any
samples involved shall be reanalyzed, if possible. If the sample cannot be reanalyzed, or if
the quality control results continue to fall outside established limits or indicate an analytical
problem, the results shall be qualified as such. Ref: 15A NCAC 02H .0805 (g) (8)..
Requirement: A post-check verification can be performed with the initial calibration value in
mind. If, for instance, you calibrate your instrument to 98% and then conduct your DO
testing, you can place the sensor back into the same calibration environment and it should
read +/- 2% (+/- 1% on optical) of 98% once stable. Ref: YSI, Dissolved Oxygen Meters
Q&A | The Ultimate List Patrick Higgins | Jan 31, 2017.
Requirement: Calibration: Follow manufacturer’s calibration procedure exactly to obtain
guaranteed precision and accuracy. Ref: Standard Methods, 4500 O G-2011. (3) (a).
Comment: The laboratory performs the calibration and post-analysis calibration verifications
on the DO meter using % saturation. The initial calibration values frequently show results
around 80% saturation. The post-analysis calibration verifications are usually much higher
(~98% saturation). The laboratory must investigate causes for the initial calibration value to
vary widely from the post-analysis calibration verification value.
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Temperature – Standard Methods, 2550 B-2010 (Aqueous)
I. Finding: The annual temperature-measuring device check procedure is not performed
correctly.
Requirement: Laboratory procedures shall comply with Subparagraph (a)(1) of this Rule.
Ref: 15A NCAC 02H .0805 (g) (4).
Requirement: To check a compliance temperature-measuring device, compare readings at
two temperatures that bracket the range of compliance samples routinely analyzed against a
National Institute of Standards and Technology (NIST) traceable temperature-measuring
device and record all four readings. The readings from both devices must agree within 0.5
ºC. Ref: NC WW/GW LCB Approved Procedure for the Analysis of Temperature.
Comment: The laboratory could not provide sufficient documentation that a comparison of
the compliance temperature-measuring device and a NIST thermometer was correctly
performed. Documentation contained a result of 70.1 ºF which could not be determined if it
was the compliance temperature-measuring device or the NIST thermometer.
J. Finding: Documentation of the compliance temperature-measuring device calibration
verification does not include the stated accuracy of the National Institute of Standards and
Technology (NIST) traceable temperature-measuring device that was used in the
comparison. This is considered pertinent data.
Requirement: Laboratory procedures shall comply with Subparagraph (a)(1) of this Rule.
Ref: 15A NCAC 02H .0805 (g) (4).
Requirement: All compliance temperature-measuring devices without a valid NIST
certificate must be checked initially and every 12 months against an NIST traceable
temperature-measuring device and the process documented. Documentation must include
the serial number of the device being checked. The serial number, stated accuracy and
expiration date of the NIST traceable temperature-measuring device used in the comparison
must also be documented. Verification data must be kept on file and be available for
inspection for 5 years. (NOTE: Vendors or other Certified laboratories may provide
assistance in meeting this requirement. When a vendor or other Certified laboratory provides
this assistance, they must provide a copy of their NIST Certificate or the serial number,
accuracy and calibration expiration date.) Ref: NC WW/GW LCB Approved Procedure for
the Analysis of Temperature.
Requirement: All NIST traceable temperature-measuring devices must have a stated
accuracy of at least ± 0.5°C and be within their expiration date. Ref: NC WW/GW LCB
Approved Procedure for the Analysis of Temperature.
IV. PAPER TRAIL INVESTIGATION:
The paper trail consisted of comparing original records (e.g., laboratory benchsheets, logbooks, etc.)
and contract laboratory reports to Discharge Monitoring Reports (DMRs) submitted to the North Carolina
Division of Water Resources. Data were reviewed for RDU Airport Authority (NC General Permit #
NCS000588) for March 2017, January 2021 and March 2021. No transcription errors were observed.
The facility appears to be doing a good job of accurately transcribing data.
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V. CONCLUSIONS:
Correcting the above-cited Findings will help this laboratory to produce quality data and meet
Certification requirements. The inspector would like to thank the staff for their assistance during the
inspection and data review process. Please respond to all Findings and include supporting
documentation, implementation dates and steps taken to prevent recurrence for each corrective
action.
Report prepared by: Tom Halvosa Date: July 21, 2021
Report reviewed by: Tonja Springer Date: July 26, 2021
Certificate Number:5253
Effective Date:1/1/2021
Expiration Date:12/31/2021
Lab Name:RDU Airport Authority
Address:1000 Trade Drive
RDU Airport, NC 27623
North Carolina Wastewater/Groundwater Laboratory Certification
Certified Parameters Listing
Date of Last Amendment:
The above named laboratory, having duly met the requirements of 15A NCAC 2H.0800, is hereby certified for the measurement of the parameters listed below.
CERTIFIED PARAMETERS
INORGANIC
DISSOLVED OXYGEN
SM 4500 O G-2011 (Aqueous)
pH
SM 4500 H+B-2011 (Aqueous)
TEMPERATURE
SM 2550 B-2010 (Aqueous)
This certification requires maintance of an acceptable quality assurance program, use of approved methodology, and satisfactory performance on evaluation samples. Laboratories are subject to civil penalties and/or decertification for infractions
as set forth in 15A NCAC 2H.0807.