1). When a QAE finds a defect on a single product does the QAE continue to look for other defects on that single product to determine if the AQL is exceeded or is the intent of the AQL to determine if, as in this case, a total of 2 individual units were defective?
2) With this statement in the contract, is the QALI the controlling document for accepting or rejecting or should we be using Zero Based sampling?
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The consensus is the QAS should contact their supervisor for guidance.