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Warning Letters | FDA Learn about the types of warning letters on FDA's website Matters described in FDA warning letters may have been subject to subsequent interaction between FDA and the letter
FDA Warning Letters - Pharmaguideline Warning letter are an official message from United States Food and Drug Administration to the pharmaceutical manufacturers about the violation of cGMP and other regulatory rules
FDA warns Canadian firm for hostile behavior during . . . In a warning letter sent to Brand International Corporation, located in Ontario, Canada on 17 December, FDA detailed several egregious issues, including limiting and obstructing an inspection in violation section 501 (j) of the Federal Food, Drug, and Cosmetic Act
U. S. Food and Drug Administration FDA Food and Beverage Recall tonnage for 2016 Entire U S recalled food and beverage recall tonnage, by manufacture origin, if possible 01 01 2016 - 12 01 2016
FDA sends Warning Letter to Canadian OTC Manufacturer - ECA . . . A manufacturer of over-the-counter (OTC) drug products based in Canada received a Warning Letter from the U S Food and Drug Administration (FDA) regarding significant violations of Current Good Manufacturing Practice (CGMP) regulations for finished pharmaceuticals
FDA Warning Letters Tracker - LexisNexis This tracker highlights selected drug and medical device-focused warning letters issued by the FDA in response to FDA’s determination that a manufacturer has violated, or potentially violated, applicable requirements of the Food, Drug, and Cosmetics Act (FDCA), FDA regulations, or agency guidance