Can an organization be certified by a 3rd party to AS9102B in the same fashion as they might be certified to AS9100C?
QMS process interaction map
"Sir, We recently went through the AS9100 audit and was wrote up for our QMS process interaction map not having the correct reference. Does this fall into the "no mandatory documents being required?" Please explain what "no mandatory documents being required."
Main focus for AS9100 Rev D product realisation
what are the main things to be focused in AS9100 standards. from product realization point of view
Conducting AS9100D internal audits
CONDUCTING AS9100D INTERNAL AUDITS AS PER ORGANISATION QMS MANUAL AND PROCEDURES ARE ACCEPTABLE? OR INTERNAL AUDITS TO BE CONDUCTED ONLY AS PER AS9100D STANDARD. PLEASE ADVISE.
Gap Analysis AS9100 Rev C vs Rev D
"Please provide gap analysis btw AS rev c and AS rev d"
Internal Audit Impartiality
"Is it okay to assign NDT Responsible Level 3 to perform internal audit at NDT area? "
AS9100D clause 8.4.2.d
"I am representing a small family owned company injection molding company in Southern Vermont who is attempting to be certified to AS9100 Rev D.
AS9100 Internal Audit Frequency
"Good Morning Mark,
Clause 4 in ISO 9001:2015 and AS9100 Rev D
About clause 4 of the new ISO9001:2015. what is needed to fulfill this requirement? I am already ISO and AS so how does this cross reference with the 2008?
Is research & development part of Design & development?
I would like to know if you need to document. Or how I would document research and development stage. Under ISO9001:2015 / AS9100D does this fall under Design and development and if so where in the SAE is that stated?