1) Are they still in our factory?
2) If yes, all of them should be rejected.
3) If no, frankly speaking, I am in doubt for our QA/QC system. Can we recall products?
4) Either 2 or 3 above, it must be detected by our QA/QC system, not until it has been reported thru after inventory checking.
Saran/WA, please review your sampling plan. Why could we detect via QA/QC?
Nittaya/WA, please carefully investigate this. If necessary, please issue CPAR and follow up for root cause/corrective and preventive actions/effectiveness.
If you have any reason to explain, please do it.