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.

What Happens If You Make Cosmetic, OTC Drug, or Dietary Supplement with Hemp, Cannabis, or THC – Part Two

Healthcare makers, distributors, and sellers must comply with FDA rules and warning letters for their cannabis, hemp, and THC products including foods, OTC drugs, cosmetics, and dietary supplements

What Happens If You Make a Food with Hemp, Cannabis, or THC – Part One

Healthcare makers, distributors, and sellers must comply with FDA rules and warning letters for their cannabis, hemp, and THC products including foods, OTC drugs, cosmetics, and dietary supplements

Why Medical Device Companies Need to Fear FDA Warning Letters

The FDA examines whether medical devices comply with the regulations of the Food, Drug, and Cosmetic Act. Two of the most common violations medical device companies are charged are adulteration [...]