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ARCHIVED REPORTS_XR0012599
EnvironmentalHealth
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EHD Program Facility Records by Street Name
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MOFFAT
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3500 - Local Oversight Program
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PR0545574
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ARCHIVED REPORTS_XR0012599
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Entry Properties
Last modified
10/12/2020 11:00:40 PM
Creation date
3/19/2020 1:36:51 PM
Metadata
Fields
Template:
EHD - Public
ProgramCode
3500 - Local Oversight Program
File Section
ARCHIVED REPORTS
FileName_PostFix
XR0012599
RECORD_ID
PR0545574
PE
3528
FACILITY_ID
FA0006135
FACILITY_NAME
PONY EXPRESS COURIER CORP
STREET_NUMBER
959
STREET_NAME
MOFFAT
STREET_TYPE
BLVD
City
MANTECA
Zip
95336
CURRENT_STATUS
02
SITE_LOCATION
959 MOFFAT BLVD
P_LOCATION
04
P_DISTRICT
005
QC Status
Approved
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SJGOV\sballwahn
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EHD - Public
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.. xu a'i .. ., •. a R� �_-, y '� �^ .-nom � � �-, r• ��-�o srp nr rr Vd�^�� - sa �� <br /> SHERWOOD LABS CORPORATION <br /> Ouality Control Program <br /> Page : 4 <br /> 4. DETECTOR PERFORMANCE <br /> The following items are monitored to evaluate the performance <br /> of detectors: <br /> a. Linearity results compiled from qualified standards. <br /> b. Monitoring standard response factors, <br /> c. Monitoring baseline voltage. <br /> Problems that can be isolated as originating with the detector <br /> are approached according to the manufacturers' recommendations <br /> for diagnostics and corective action. If recommended actions <br /> do not correct detector performance repairs and recalibrations <br /> are performed by a factory representative. <br /> 5. AUTOSAMPLER PERFORMANCE <br /> Evaluation of the autosampler includes procedures intended to <br /> determine the validity of sample loading by personnel <br /> responsible for analyses and instrument operation and the <br /> performance characteristics of the autosampler. The following <br /> r <br /> items are monitored as pat of the autosampler evaluation <br /> process: <br /> a. visual examination of all vials to insure that volumes of <br /> remaining liquid are the same. Lack of uniformity <br /> indicates autosampler mechanical problems and will result <br /> in the rerunning of the sample batch, Further use of the <br /> autosampler will be suspended until the problem is <br /> corrected. The problem will be considered resolved if <br /> sample vials contain un f^rm levels of liquid after <br /> of standards is satisfactory <br /> analysis and repeatabilit% <br /> ( see STANDARDS - repeatability guidelines ) . <br /> b. tDurng he�loo tion of removal <br /> theovial sample <br /> id vial vials <br /> IDfrom <br /> arethe <br /> autosampler <br /> carefully <br /> compared with the information read toes fple ID and of the <br /> position on the autosample log pages. <br /> correctness of this log is required as part of the data <br /> validation process- that -i s- completed prior toSubmission <br /> of customer results. <br />
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