Validation Deviation

During an Equipment IOQ, how is the Validation Deviation / non-conformance recorded? In QMS? Or do you use a Validation Deviation SOP that has QA oversite, but keeps this type of non-conformance out of QMS since equipment is not yet “qualified”. An example would be a CPP - Critical Process Parameter passing criteria was not met during OQ. Would you call this a “Validation Deviation”, a " non-conformance", an “event”, an “incident”? Thanks!

You can record it as a outstanding point in the comments section or deviation section of the datasheet itself, meanwhile further activity can be proceeded…
Corrective action shall be proposed as then action shall be taken accordingly…
The outstanding report shall be closed upon completion of action…
Thanks