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MPLOYEE S SIGNAnJRE SEE REVERSE OF THIS PAGe x-- ORM FDA 183 9/08 PREVIOUS EDITION Oi3SOLETE EMPLOYEE NAME AN D nTLE Rinl or Type N clto/u c.. 6 Cream Failed sent for re-test Estriol re-test 7/15/14 106. 2 Passed 2 origina l 10/20/2014 06-25 2014 45 07 152014 41 re test 11/26/14 2014 10 Progesterone original 2014 32 138. 075 gms 0. 032 7/20/16. T3 required inRx Your firm b 4 T3 b 4 lot b 4 for the T3 in the following abovementioned prescriptions on 7/ 6/ 16. Specitically Observation 1 T3 in...
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The Food and Drug Administration is a federal agency responsible for protecting and promoting public health through the control and supervision of food safety, drug safety, and other medical products.
Manufacturers, importers, and distributors of food and drug products are required to file with the Food and Drug Administration.
To fill out the Food and Drug Administration form, companies must provide detailed information about their products, including ingredients, manufacturing processes, and safety testing results.
The purpose of the Food and Drug Administration is to ensure the safety and efficacy of food and drug products available to the public.
Information such as product ingredients, manufacturing processes, safety testing results, and any known side effects or warnings must be reported on the Food and Drug Administration form.
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