Common use of Product Sampling Clause in Contracts

Product Sampling. 3.1 Visual Inspection Each Finished Product lot shall be randomly sampled in accordance with ANSI/ASQ Z1.4, current revision, General, Inspection Level II, Single Normal Sample 0.65 AQL (unless otherwise instructed by Quality Assurance Management), with specific notes for intolerable, major and minor defects (see section 4.0 “Visual Classification of Defects”). Results shall be recorded on appropriate Work Instructions. A lot is defined as the quantity of product processed from one DBM Donor lot and manufactured within a single production record. 3.2 Endotoxin Testing (LAL) LAL test samples, representative of final product, shall be submitted to an approved test laboratory in accordance with section 5.2.

Product Sampling. 3.1 Visual Inspection Each Finished Product lot shall be randomly sampled in accordance with ANSI/ASQ Z1.4, current revision, General, General Inspection Level II, Single Normal Sample 0.65 AQL (unless otherwise instructed by Quality Assurance Management), with specific notes for intolerable, major and minor defects (see section 4.0 “Visual Classification of Defects”). Results shall be recorded on appropriate Work Instructions. A lot is defined as the quantity of product processed from one DBM Donor lot and manufactured within a single production record. 3.2 Endotoxin Testing (LAL) LAL test samples, representative of final product, shall be submitted to an approved test laboratory in accordance with section 5.2.

Product Sampling. 3.1 Visual Inspection Each Finished Product lot shall be randomly sampled in accordance with ANSI/ASQ Z1.4, current revision, General, General Inspection Level II, Single Normal Sample 0.65 AQL (unless otherwise instructed by Quality Assurance Management), with specific notes for intolerable, major and minor defects (see section 4.0 “Visual Classification of Defects”). Results shall be recorded on appropriate approved applicable Work InstructionsInstruction. A lot is defined as the quantity of product processed from one DBM Donor donor lot and manufactured within a single production record. 3.2 Endotoxin Testing (LAL) LAL test samples, representative of final product, shall be submitted to an approved test laboratory in accordance with section 5.26.2. Document sample removal on Form-118.