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It is still difficult for systems designers to build machines that allow finished products to be inspected easily. To do so requires an understanding of the product being manufactured and how inspection tasks can improve the quality control process. [3] Inspection can represent a significant percentage of an existing product's manufacturing cost.
Facility condition assessment is an analysis of the condition of a facility in terms of age, design, construction methods, and materials. [1] [2] The individuals who perform the assessment are typically architects and engineers, and skilled-trade technicians.
A copy of the AAI (Appearance Approval Inspection) form signed by the customer. Applicable for components affecting appearance only. Sample Production Parts A sample from the same lot of initial production run. The PPAP package usually shows a picture of the sample and where it is kept (customer or supplier). Master Sample
A template is a device used by sanctioning body officials to check the body shape and height of racing vehicles. [1] The template is used to check that teams have manufactured the sheet metal used in the vehicle bodies to within tight tolerances (up to thousandths of an inch).
The U.S. Food and Drug Administration (FDA) is authorized to perform inspections under the Federal Food, Drug, and Cosmetic Act, Sec. 704 (21 USC §374) "Factory Inspection". [1] Form FDA 483 , [ 2 ] "Inspectional Observations", is a form used by the FDA to document and communicate concerns discovered during these inspections.
First article inspection is typically a purchase order requirement of the purchaser for the supplier to complete. If the manufacturer doesn't have the in-house capability or if the purchaser requests, the first article inspection may be conducted by an approved subcontract supplier such as a dimensional inspection/metrology laboratory.