Is instrument ID required in the in-process inspection report per AS9100C

H

HK PRASHANTHA

Is instrument ID no. is required in the inprocess inspection report??? as per AS9100C
 

Marc

Fully vaccinated are you?
Leader
These posts were accidentally moved by a moderator. Does anyone know what thread they were in?
 

harry

Trusted Information Resource
These posts were accidentally moved by a moderator. Does anyone know what thread they were in?

These two posts were originally posted in the 'An Elsmar Cove Forum Software 'Quick Start' Guide' thread and the whole thread was moved (must had been accidentally moved) to the AS forum.

I moved the whole thread back and then moved these two posts to the AS forum.
 

somashekar

Leader
Admin
Is instrument ID no. is required in the inprocess inspection report??? as per AS9100C
The use of the unique identification of the measuring equipment in the in-process inspection report itself shows a good interaction between the inspection process and the calibration process.
Now you take a decision yourself about your requirement.
 
A

andygr

As others have indicated it is not required by the standard. Time is money and ther should always be a benifit to what you do.

It is all just a mater of risk. Why, what and who are you doing/using the FAI for. I treat a FAI like the QA version of an engineering qualification. I like to have the ability to really know what was checked and how it was done. I usually balance the additional detail inclusion of any type into the report against what the item is -critical, tight tolerance such as a gear vrs a simple electrical box.
I personally like a lot of data but the reality is you have to balance time and such and in some cases the ONLY reason FAI is being created is because it has to be and it is really nothing more than a filled out form shoved into a file.

Things to think about
What if at some point during a calibration a year down the line you discover a tool being calibrated is received out of tolerance? Can you determine if it was used on any FAI inspection?
Your Customer gets your FAI report and verifies some dimensions and indicates that they get different readings. Would it not be nice to match your actual inspection tool deviation from nominal against their data to see if the instruments are on opposite side of the tolerance band?

:2cents:
 

dsanabria

Quite Involved in Discussions
Is instrument ID no. is required in the inprocess inspection report??? as per AS9100C

The only time that the standards requires that you provide measurements of intruments is when the product is accepted (i.e. Final Inspection). If that final inspection is done at in-process... then.

Clause 8.2.4

Measurement requirements for product acceptance shall be documented and shall include

d) any specific measurement instruments required and any specific instructions associated with their use.
 
Thread starter Similar threads Forum Replies Date
B AMS2750 Secondary Instrument, what am I doing wrong? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
D Comparing inline Conductivity instrument with offline test results General Measurement Device and Calibration Topics 0
R Clinical evaluation for instrument of a navigation system EU Medical Device Regulations 1
G AMS 2750 F Instrument Calibration Results and Recording AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
WEAVER Can you determine exact date an instrument went out of tolerance? General Measurement Device and Calibration Topics 10
R Suggest modern equipment/instrument for plastic bottle inspection? Quality Tools, Improvement and Analysis 1
H California Instrument AC Load - 222 Error Message Manufacturing and Related Processes 0
N 60601-2-2 Ed 6 Clause 201.8.8.3.102 - HF instrument leakage IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
J Reusable surgical Instrument is under class IIa? EU Medical Device Regulations 4
drwallice Surgical Instrument Tray Classification EU Medical Device Regulations 7
J IVD instrument as an accessory EU Medical Device Regulations 3
M What kind of instrument that must be calibrated? General Measurement Device and Calibration Topics 3
F What is 'floor' in an instrument's specs Measurement Uncertainty (MU) 5
B Bioburden monitoring for surgical instrument provided non-sterile EU Medical Device Regulations 3
G Is it common to do a repeatability check during calibration of an instrument? General Measurement Device and Calibration Topics 5
M Informational Is my device a Reusable Surgical Instrument under the EU MDR(2017/745)? Medical Device and FDA Regulations and Standards News 0
A MSA When an Instrument Measures More than One Parameter Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 7
J IEC 60601-2-2 - EMC Requirements - Surgical instrument manufacturer IEC 60601 - Medical Electrical Equipment Safety Standards Series 6
S Cannot create Rejects for TMV on a medical instrument with an LCD Other Medical Device and Orthopedic Related Topics 10
Q AMS 2750E Sensitivity Requirements Field Test Instrument AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
Q Guidance regarding Legally Refurbishing a Non-RoHS Instrument in the EU REACH and RoHS Conversations 1
chris1price Calibration of Instrument before being Discarded General Measurement Device and Calibration Topics 9
D AMS 2750E - Digital Instrument Calibration Accuracy Requirements General Measurement Device and Calibration Topics 1
C MSA (Measurement System Analysis) - Instrument Selection Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 4
M Kaye Instrument 373 RTD Monitor Resistance Curve General Measurement Device and Calibration Topics 2
S GR&R for an "R" value instrument installed on my 10K Horizontal Tester Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 5
G 2 Unacceptable GR&Rs - What instrument to use? General Measurement Device and Calibration Topics 15
S Can Calibration of an instrument substitute for Validation (IQ, OQ,PQ)? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
B For a measuring instrument, should MSA be done first or the Capability studies? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 4
B Total Resolution of an Measurement Instrument Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 1
M Leakage Current Measuring Instrument - IEC 60601-1 Requirement IEC 60601 - Medical Electrical Equipment Safety Standards Series 5
S Protocol of water activity measurement and suitable instrument Food Safety - ISO 22000, HACCP (21 CFR 120) 1
A How to read an analog instrument during calibration Measurement Uncertainty (MU) 2
WEAVER Calibration of Measuring Instrument by Adjustment of its Scales IATF 16949 - Automotive Quality Systems Standard 2
R How do I extend Correction factor of Calibration cert to compute instrument accuracy Measurement Uncertainty (MU) 1
D Records Requirement - Daily Instrument Verification IATF 16949 - Automotive Quality Systems Standard 5
L Tapes and Multimeters - Identification on Instrument General Measurement Device and Calibration Topics 4
H Continuous Monitoring Instrument Data Validation and how to calculate Outliers Quality Tools, Improvement and Analysis 1
R MDR Reporting for event with RUO instrument 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
1 Reprocessing of Surgical Instrument Sets Other Medical Device and Orthopedic Related Topics 4
S Instrument Calibration Laboratory setup for API Pharmaceutical Company General Measurement Device and Calibration Topics 1
C A better Instrument (Measurement Device) Identification System Misc. Quality Assurance and Business Systems Related Topics 7
C Reusable Instrument Sterilization Method Validations Other Medical Device and Orthopedic Related Topics 3
B Repeatability vs. Instrument Specifications Measurement Uncertainty (MU) 6
B AMS 2750 Furnace Instrument Calibration Operating Range AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
D Determining Instrument Purchase based on Accuracy (Micrometer) General Measurement Device and Calibration Topics 3
W Is a Non-Automatic Weighing Instrument a Medical Device? IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
D RUO (Research Use Only - Laboratory Instrument) CE Marking Requirements 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
S Surgical Instrument Luminaries Standards - Single Use Disposable Surgical Instrument IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
L Stainless Steel Grades - Nomenclature for Surgical Instrument Stainless Steel ISO 13485:2016 - Medical Device Quality Management Systems 2

Similar threads

Top Bottom