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On July 26, 2013, the FDA published for public com‐ ment its proposed rule to establish a program for accreditaƟon of third‐party auditors, also known as cerƟficaƟon bodies, to conduct food safety audits and issue cerƟficaƟons of foreign faciliƟes and the foods for humans and animals they produce. The proposed rule would implement SecƟon 307 of the FDA Food Safety Continue Reading

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FDA’s mandatory food recall authority went into effect when FSMA was enacted on January 4, 2011. Section 423 of the FD&C Act, as added by Section 206 of FSMA, gives FDA the authority to order a responsible party to recall an article of food where FDA determines that there is a reasonable probability that the article of food (other than infant formula) is adulterated under section 402 of the FD&C Act [21 U.S.C. § 342] or misbranded under section 403(w) of the FD&C Act [21 U.S.C. § 343(w)] and that the use of or exposure to such article will cause serious adverse health consequences or death to humans or animals (SAHCODHA).

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Thinking SMARTER NOT HARDER as you will see in this video line automation showcasing quality control and labeling of cartons. Automation line by www.casiusa.com offers throughput of 23.7 boxes per minute.  In the first segment, you will notice one box was sent down the line without the lid. This was done to show the reject function. Label and data collection produced Continue Reading

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This final rule affirms the IFR’s change to FDA’s records access as required by the FDA Food Safety Modernization Act (FSMA).

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There is so much focus right now on the seven proposed rules under comment and pending final rule making that it’s easy to lose sight that some powerful provisions of the Food Safety Modernization Act (FSMA) are alive and kicking well before the proposed rules become final.  For example, you may want to consider the food facility registration suspension of Roos Continue Reading

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“5 log reduction #pathogens in seconds, and a prevention step to record for #FSMA records.” http://buff.ly/1kXfC3I #foodsafety

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