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The Daily Intake

Legal and Regulatory updates for the food and supplement industry

Inspection

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USDA FSIS Implements Directives to Inspection Program Personnel as Cell-Cultured Meats Begin to Enter the U.S. Market.

Posted on July 19, 2023
  • Cell-cultured meat, also known as cultured meat, involves the production of meat from animal cells in a controlled environment. It has the potential to revolutionize the food industry by offering
… Continue Reading USDA FSIS Implements Directives to Inspection Program Personnel as Cell-Cultured Meats Begin to Enter the U.S. Market.

FDA Issues Final Guidance on Refusal of Inspection by a Foreign Food Establishment or Foreign Government

Posted on October 21, 2022
  • On October 20, FDA issued final guidance that describes the actions, behaviors, and statements by a foreign food establishment or foreign government that the FDA considers to be a refusal

…
Continue Reading FDA Issues Final Guidance on Refusal of Inspection by a Foreign Food Establishment or Foreign Government

FDA and CDC Collaborate to Develop a Process that Would Govern How to Return to On-site Facility Surveillance Inspections

Posted on May 14, 2020
  • On May 11, 2020, the U.S. Food and Drug Administration (FDA) provided an update in regard to the agency’s surveillance inspections during the COVID-19 pandemic.  In its update, FDA stated

…
Continue Reading FDA and CDC Collaborate to Develop a Process that Would Govern How to Return to On-site Facility Surveillance Inspections

FDA Increases FSVP Enforcement

Posted on April 24, 2020
  • FDA appears to have stepped up its enforcement of Foreign Supplier Verification (FSVP) regulations in the past several weeks, issuing four warning letters to companies in the past month for

…
Continue Reading FDA Increases FSVP Enforcement

FDA Publishes Draft Guidance Concerning “Refusal of Inspection”

Posted on December 11, 2017
  • Section 807(b) of the Federal Food, Drug, and Cosmetic Act, added by section 306 of the Food Safety Modernization Act (FSMA) authorizes the U.S. Food and Drug Administration (FDA) to

…
Continue Reading FDA Publishes Draft Guidance Concerning “Refusal of Inspection”

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Keller and Heckman, founded in 1962, has a broad practice in the areas of regulatory law, public policy, and litigation, serving both domestic and international clients. Our firm is a pioneer in the use of interdisciplinary approaches to problem-solving. Since 1971, we have had an in-house scientific staff that works closely with the firm’s attorneys on matters of technical complexity. Many of our attorneys also have government experience and expertise in multiple areas of the law.

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