FDA Warns Foreign Maker of a Hand Sanitizer Product That Its Product is Adulterated
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FDA Warns Foreign Maker of a Hand Sanitizer Product That Its Product is Adulterated

The Food and Drug Administration issued a warning letter to a foreign manufacturer that the substation of methanol for ethanol rendered its produce a new drug, adulterated, and misbranded.

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 US FDA Sends Warning Letter to Red Pill Medical That Its CBD Dietary Supplements Violate FDA Rules
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US FDA Sends Warning Letter to Red Pill Medical That Its CBD Dietary Supplements Violate FDA Rules

FDA sends out another warning letter to CBD companies that promote that company products for medical uses and for treating diseases will be in violation of the FD&A Act.

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 Federal District Court Orders New York Company to Stop Distributing Adulterated and Misbranded Dietary Supplements
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Federal District Court Orders New York Company to Stop Distributing Adulterated and Misbranded Dietary Supplements

FDA enforcement warning letters sent to manufacturers of CBD based dietary supplements due to non-permissible misbranding and adulteration claims

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 FDA Warning Letters To Companies Claiming Products Boost Immunity and Treat COVID-19
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FDA Warning Letters To Companies Claiming Products Boost Immunity and Treat COVID-19

Federal Drug Administration continues to send warning letters to companies that boast products can treat, diagnose, prevent, or cure COVID-19 or boost immunity.

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 FDA Warning Letters Sent to Companies That Claim Products are Effective against COVID-19
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FDA Warning Letters Sent to Companies That Claim Products are Effective against COVID-19

Federal Drug Administration has started sending warning letters to companies that boast their products can treat, diagnose, prevent, or cure COVID-19 or boost immunity.

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