12 Calibration
12 Calibration
Process Name
Calibration
Document No
FVMT/QA/QP/12
Amendment Record
1. PURPOSE :- To describe the system for control , calibration & maintenance of Gauges/Measuring equipment's & instruments & test
Equipment's.
2. SCOPE :- The process is applicable to all the Gauges/Measuring equipment's & instruments & test Equipment's.Related to flash
owned,customer owned and onsite supplier owned instruments/equipments.
3. DOCUMENT REFERENCE :-
3 Acceptance criteria
4 SWP MSA
4. ABBEREVATIONS :- NIL
5. RECORDS :-
6. KPI :-
100% Adherence to calibration plan As per KPI List Monthly Lab QA Engineer
7. INTER-RELATED PROCESS :-
PROCESS NAME
Production control process
PAGE : 1 of 4
Document No:
QUALITY MANAGEMENT SYSTEM Issue Date 08.07.2020
FVMT/QA/QP/12 Revision No. 01
Process Name Revision Date 06.07.2020
Calibration
Document/Record Reference/
Input/ Trigger Responsibility Activity
Generated Instructions
Input
10 10
*Calibration plan - 10 - 200 IPO/Control plan
Quality Engineer Determine the monitoring & measurement to be made & appropriate
Past data
monitoring & measuring equipment with required accuracy based on drgs,
*List of gauges,
mfg. test specification, process specification etc.
Instruments &
equipment's 20 20
*Tolerance/spec. Tooling
of characteristic Procure monitoring & measuring equipment Management
customer 30 (Section 1)
requirement Receive monitoring & measuring equipment
*Acceptance
criteria 40
*Identification-
gauges, Is the measuring & monitoring
Instruments & equipment a new one?
equipment's
*National / 50 Yes New
International No Existing
standard
*List of Manufacturer calibration certificate available?
accredited lab 60
60
Calibrate using an accredited 70
List of accredited
lab or non-accredited lab if Obtain calibration certificate from calibration agency
approved by Head-QA or Mfg../supplier
customer
80
Do the calibration 80
No
result meet Acceptance Criteria
acceptance criteria? 90 No
Return the
B Gauge/Instrument to
Yes Yes supplier
100 110
140
150
Issue the gauge/instrument to
user with status sticker & colour
coding as per calibration colour 140
code Decide the calibration interval 1.Gauge
160 Requisition & issue
Slip
Protect from 170 2.Calibration colour
damage/deterioration during code
handling/storage Safeguard from adjustment
if any gauge/instrument
damage/lost withdrawn from 160
180
the use & filled gauge
Gauge Requisition
requisition slip from user
& issue Slip
Issue to user as required
190
Review the list of 200
gauges/instruments monthly
for calibration status against Update gauges/Instrument list & 190
schedule calibration plan Master list of
calibration due expire calibration list
gauges/instrument to be
PAGE : 2 of 4
Document No:
QUALITY MANAGEMENT SYSTEM Issue Date 08.07.2020
FVMT/QA/QP/12 Revision No. 01
Process Name Revision Date 06.07.2020
Calibration
Document/Record Reference/
Input/ Trigger Responsibility Activity
Generated Instructions
A
210
210
Calibration
Maintain calibration records including Certificate
-Equipment identification, measurement of standards
-Revision following engineering change
-Any out of spec. readings as received during calibration
-Calibration certificate from supplier
210-270 -Assessment of conformity after calibration
Quality Engineer -Verification of the software version
220
220
Verification of Master, special gauges & instruments frequently 1. Gauge
as per plan. Verification Report
230
2. Instrument
MSA SWP
Verification report
230
B
240
250
260
Take appropriate action on the parts/products
produced using the "Out of calibration"
equipment/instrument/gauge
270
PAGE : 3 of 4
QUALITY SYSTEM PROCESS
Document No. FVMT/QA/QP/12
(Turtle Diagram)
IATF16949 Revision No. 01
7.1.5.2.1,7.1.5.3.1,7.1.5.2,7.1. Process : Calibration
5.1.1,7.1.5.3.2
Revision Date 06.07.2020
Inputs
* Calibration Plan - Past Data Process
* List of Gauges, Instruments & Outputs
Equipment's
* Tolerance/Spec. of customer
characteristics
*Acceptance Criteria
Calibration - Gauges, *Calibrated Gauges / Instrument /
*Identification-Gauges, Instruments & Instruments, Electronic Equipment meeting acceptance criteria
Equipment's equipment's
*National/International Standard
* List of accredited lab
PAGE : 4 of 4
Annexure-1 -FVMT/QA/QP/12
FV/STD/A1/DM-01
STANDARD ROOM (LOCATION) DIGITAL OD MIC
LEAST COUNT OF MME
RANGE OF MME