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NC Department of Environmental Quality | Division of Water Resources | Laboratory Certification Branch
4405 Reedy Creek Road | 1623 Mail Service Center | Raleigh, North Carolina 27699-1623
919-733-3908
June 21, 2023
5117
Mr. Brandon Johnson
Town of Angier WWTP
P.O. Box 278
Angier, NC 27501-
Subject: North Carolina Wastewater/Groundwater Laboratory Certification Branch (NC
WW/GW LCB) Maintenance Inspection
Dear Mr. Johnson:
Enclosed is a report for the inspection performed on May 23, 2023 by Tonja Springer. 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 02H .0800.
A copy of the laboratory’s Certified Parameter List at the time of the audit is attached. This list will
not 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, Tonja Springer, #5117
On-Site Inspection Report
LABORATORY NAME: Town of Angier WWTP
WATER QUALITY PERMIT #: WQ0002638
ADDRESS: 420 Campbell Street
Angier, NC 27501
CERTIFICATE #: 5117
DATE OF INSPECTION: May 23, 2023
TYPE OF INSPECTION: Field Municipal Maintenance
AUDITOR(S): Tonja Springer
LOCAL PERSON(S) CONTACTED:
Brandon Johnson
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. The
analyst was forthcoming and responded well to suggestions from the auditor.
All required Proficiency Testing (PT) Samples for the 2023 PT Calendar Year have not yet been analyzed.
The laboratory is reminded that results must be received by this office directly from the vendor by September
30, 2023.
Any time changes are made to laboratory procedures, Quality Assurance (QA) and/or Standard Operating
Procedure (SOP) document(s) must be updated and relevant staff retrained. Staff must acknowledge that
they have read and understand the changes as part of the documented training program. The same
requirements apply when changes are made in response to Findings, Recommendations or Comments
listed in this report, to ensure the methods are 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
instances, the laboratory may need to create an SOP to document how new functions or policies will be
implemented. Revisions to the SOPs, based on the Findings, Comments and Recommendations
within this report must be submitted to this office by December 31, 2023.
The laboratory is 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”.
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Contracted analyses are performed by Pace Analytical Services LLC - Huntersville NC (Certification # 12).
Approved Procedure documents for the analysis of the facility’s currently certified Field Parameters were
provided at the time of the inspection.
III. FINDINGS, REQUIREMENTS, COMMENTS AND RECOMMENDATIONS:
Comment: The facility has a Non-discharge Surface Irrigation permit. At the time of the inspection,
no spray events had occurred since April 2022. Only 2022 Proficiency Testing (PT) data were
available for review.
Documentation
Recommendation: It is recommended that the name of the PT study be documented (e.g., NSI WP-
272) in the space provided for Facility/Sample location. The facility name is already documented at
the top of the benchsheet.
Recommendation: The make and model of the meter is documented on the benchsheet for the
instrument identification. It is recommended to include the serial number of the meter.
Comment: Chemical containers are not dated when opened. North Carolina Administrative Code, 5A
NCAC 02H .0805 (g) (7) states: Chemical containers shall be dated when received and when opened.
Ref: 15A NCAC 02H .0805 (g) (7). Acceptable corrective action was taken at the time of the inspection
(i.e., the date opened was documented on the reagent containers currently in use). No further
response is necessary for this Corrected Finding.
Comment: The three gel-type standard values used to assign the true value are not documented.
North Carolina Administrative Code, 5A NCAC 02H .0805 (g) (1) states: All analytical records,
including original observations and information necessary to facilitate historical reconstruction of the
calculated results, shall be maintained for five years. All analytical data and records pertinent to each
certified analysis shall be available for inspection upon request. The NC WW/GW LCB Approved
Procedure for the Analysis of Total Residual Chlorine document states: To assign a true value to the
gel-type or sealed liquid standard: 1. Zero the instrument with the calibration blank. 2. Read and
record gel standard values. 3. Repeat steps 1 and 2 at least two more times. 4. Assign the average
value as the true value. Acceptable corrective action was taken at the time of the inspection (i.e., the
gel standard was read three times and readings documented and gel standard assigned a new true
value). No further response is necessary for this Corrected Finding.
A. Finding: The laboratory is lacking a documented training program.
Requirement: Each laboratory shall develop and implement a documented training program
that includes the following: that staff have the education, training, experience, or demonstrated
skills needed to generate quality control results within method-specified limits and that meet
the requirements of these Rules; that staff have read the laboratory quality assurance manual
or applicable Standard Operating Procedures; that staff have obtained acceptable results on
Proficiency Testing Samples pursuant to Rule .0803(1) of this Section or other demonstrations
of proficiency (e.g., side-by-side comparison with a trained analyst, acceptable results on a
single-blind performance evaluation sample, an initial demonstration of capability study
prescribed by the reference method). Ref: 15A NCAC 02H .0805 (g) (5).
B. Finding: The laboratory benchsheet does not reference the currently approved methods.
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Requirement: Laboratory procedures shall comply with Subparagraph (a) (1) of this Rule.
Ref: 15A NCAC 02H .0805 (g) (4).
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. Ref: 15A NCAC 02H .0805 (g) (2) (A).
Comment: The methods are documented as follows on the benchsheets: Total Residual
Chlorine (TRC) SM 4500 Cl G -2000 and pH SM 4500 H+B-2000. The Standard Methods
references must be updated to the currently approved and certified method.
C. Finding: The laboratory is not documenting the assessment of QC standards on the
laboratory benchsheet.
Requirement: All laboratories shall use printable laboratory benchsheets. Certified Data shall
be traceable to the associated sample analyses and shall consist of: the quality control
assessments. Each item shall be recorded each time samples are analyzed. Ref: 15A NCAC
02H .0805 (g) (2) (O).
Comment: This Finding applies to TRC and pH. The concentration acceptance range for the
TRC Daily Check Standard and the pH buffer check acceptance criterion are documented on
the benchsheet. There is no documentation showing that the analyst assesses the values
obtained against the acceptance ranges. A check box indicating that the acceptance criterion
has been met would satisfy this requirement. No data were observed where the QC results
were outside the acceptance criteria.
D. Finding: The units of measure for pH (i.e., Standard Units or S.U.) are not documented on
the calibration log.
Requirement: All laboratories shall use printable laboratory benchsheets. Certified Data shall
be traceable to the associated sample analyses and shall consist of: the proper units of
measure. Each item shall be recorded each time samples are analyzed. Ref: 15A NCAC 02H
.0805 (g) (2) (L).
E. Finding: The laboratory is not documenting the check standard buffer value obtained.
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 buffer. Ref: NC WW/GW LCB Approved
Procedure for the Analysis of pH.
Requirement: A record of instrument calibration or calibration verification shall be
documented and available for inspection upon request. Ref: 15A NCAC 02H .0805 (g) (3).
Requirement: The laboratory shall retain all records necessary to facilitate historical
reconstruction of the analysis and reporting of analytical results for PT Samples. This means
the laboratory must have available and retain for five years [pursuant to 15A NCAC 02H .0805
(a) (7) (E) and (g) (1)] all of the raw data, including benchsheets, instrument printouts and
calibration data, for all PT Sample analyses and the associated QC analyses conducted by
all Parameter Methods. Ref: Proficiency Testing Requirements, January 1, 2023, Revision 6,
Section 4.0.
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# 5117 Town of Angier WWTP
Proficiency Testing
F. Finding: The laboratory does not have a documented plan for PT procedures.
Requirement: Each laboratory shall develop documentation outlining the analytical quality
control practices used for the Parameter Methods included in its Certification, including
Standard Operating Procedures for each certified Parameter Method. Quality assurance,
quality control, and Standard Operating Procedure documentation shall indicate the effective
date of the document and be reviewed every two years and updated if changes in procedures
are made. Each laboratory shall have a formal process to track and document review dates
and any revisions made in all quality assurance, quality control, and Standard Operating
Procedure documents. Supporting Records shall be maintained as evidence that these
practices are implemented. The quality assurance, quality control, and Standard Operating
Procedure documents shall be available for inspection by the State Laboratory. Ref: 15A
NCAC 02H .0805 (a) (7).
Requirement: Laboratories must have a documented plan [this is usually detailed in the
laboratory’s Quality Assurance Manual or may be a separate Standard Operating Procedure
(SOP)] of how they intend to cover the applicable program requirements for Proficiency
Testing per their scope of accreditation. This plan shall cover any commercially available PT
Samples and any inter-laboratory organized studies, as applicable. The plan must also
address the laboratory’s process for submission of PT Sample results and related Corrective
Action Reports (CARs). Ref: Proficiency Testing Requirements, January 1, 2023, Revision
6, Section 3.0.
G. Finding: The laboratory is not documenting the preparation of PT Samples.
Requirement: PT Samples received as ampules are diluted according to the Accredited PT
Sample Provider’s instructions. It is important to remember to document the preparation of PT
Samples in a traceable log or other traceable format. The diluted PT Sample then becomes a
routine Compliance Sample and is added to a routine sample batch for analysis. No
documentation is needed for whole volume PT Samples which require no preparation,
however the instructions must be maintained. Ref: Proficiency Testing Requirements, January
1, 2023, Revision 6, Section 3.6.
Comment: This Finding applies to TRC.
Comment: Dating and initialing the instruction sheet for each prepared PT Sample would
satisfy the documentation requirement.
H. Finding: PT Samples are not analyzed in the same manner as routine Compliance Samples.
Requirement: Laboratories are required to analyze an appropriate PT Sample by each
Parameter Method and in each associated matrix 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
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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, January 1, 2023, Revision 6, Section 3.6.
Comment: The laboratory is currently analyzing PT Samples in duplicate and averaging the
results, which is not how Compliance Samples are treated. Sample duplicates are not required
for Field Parameters.
Quality Assurance/Quality Control (QA/QC)
I. Finding: SOPs have not been updated for all the methods included on the laboratory’s
Certified Parameters Listing (CPL).
Requirement: Laboratory procedures shall comply with Subparagraph (a)(1) of this Rule. A
copy of each analytical method or Approved Procedure and Standard Operating Procedure
shall be available to each analyst and available for review upon request by the State
Laboratory. Standard Operating Procedure documentation shall state the effective date of the
document and shall be reviewed every two years and updated if changes in procedures are
made. Each laboratory shall have a formal process to track and document review dates and
any revisions made in all Standard Operating Procedure documents. Supporting Records
shall be maintained as evidence that these practices are implemented. Ref: 15A NCAC 02H
.0805 (g) (4).
Comment: An SOP describes the method in such detail that an experienced analyst
unfamiliar with the method can obtain acceptable results and meet documentation
requirements. SOPs must describe in detail how a method is performed.
Comment: The laboratory does have an SOP for pH and TRC, but it only includes procedural
steps for the calibration and sample analysis. The laboratory must have updated QC/SOP
documents for the parameters included on their CPL by December 31, 2023. These must be
submitted for review upon completion. SOP templates were left with the laboratory at the time
of the inspection.
Total Residual Chlorine – Standard Methods, 4500 Cl G-2011 (Aqueous)
J. Finding: The laboratory is not analyzing a Method Blank when using laboratory-prepared
standards.
Requirement: Laboratory procedures shall comply with Subparagraph (a)(1) of this Rule. Ref:
15A NCAC 02H .0805 (g) (4).
Requirement: Method Blanks would be required when using laboratory-prepared standards
[including Proficiency Testing (PT) Samples] and anytime sample dilutions are performed.
Ref: NC WW/GW LCB Approved Procedure for the Analysis of Total Residual Chlorine (DPD
Colorimetric by SM 4500 Cl G-2011).
Requirement: The Method Blank is deionized or distilled water from the same source used
to prepare the calibration verification standards or the PT Sample, and is analyzed like a
sample (i.e., with DPD/buffer added). The concentration of the Method Blank must not exceed
50% of the reporting limit (i.e., the lowest calibration verification standard concentration) or
corrective action must be taken. Ref: NC WW/GW LC Approved Procedure for the Analysis
of Total Residual Chlorine (DPD Colorimetric by SM 4500 Cl G-2011).
Comment: The prepared PT Sample is considered a laboratory-prepared standard.
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IV. PAPER TRAIL INVESTIGATION:
No paper trail was conducted at the time of the inspection.
V. CONCLUSIONS:
Correcting the above-cited Findings and implementing the Recommendation(s) 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: Tonja Springer Date: June 6, 2023
Report reviewed by: Jill Puff Date: June 6, 2023
Certificate Number:5117
Effective Date:1/1/2023
Expiration Date:12/31/2023
Lab Name:Town of Angier WWTP
Address:420 Campbell Street
Angier, NC 27501-
North Carolina Wastewater/Groundwater Laboratory Certification
Certified Parameters Listing
Date of Last Amendment:7/3/2017
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
CHLORINE, TOTAL RESIDUAL
SM 4500 Cl G-2011 (Aqueous)
pH
SM 4500 H+B-2011 (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.