I have a client that has weigh scales in both their receiving department and mixing department. They use the scales for overall verification of weights when materials come in and when materials are mixed together in a vat. Although they verify that the weight measurements they are getting from the scales are in the ballpark by checking with objects of known weight, they are not concerned with the level of precision for either application. The mixed materials undergo specific visual inspections later on in the process and they have never had an issue where the mixed product had to be rejected. They have assessed the risks of mixing with a weigh scale used for reference only and have decided that the cost of verification/calibration is much more than the cost due to risk of product batch failure. Therefore, since product inspection related to proper mix of materials is carried out later on in the process, they have decided to remove the weigh stations from a calibration program and label them "not calibrated - use for reference only".
Personally, I agree with their reasoning, and their right to make this decision. As long as their product quality is protected through the product inspection later in the process, the organization should be able to weigh the risks/costs of calibration. Thier ISO 9001 Registrar may not agree.
What are your views?
Personally, I agree with their reasoning, and their right to make this decision. As long as their product quality is protected through the product inspection later in the process, the organization should be able to weigh the risks/costs of calibration. Thier ISO 9001 Registrar may not agree.
What are your views?
Here is a perfect opportunity to keep your client's system simple -- don't put the scales in and see what happens. Why complicate things? However, you are right to be concerned about your Registrar. They tried to nick us -- we never really concerned ourselves with scales. They aren't that important in our process. We had them verified once per year by the original vendor. Guess what -- they where not a ISO certified "lab." Can you say potential nightmare? These are the areas in which the registration process and standard quickly can get out of hand. I wish your client luck.
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