|
gptkbp:instanceOf
|
gptkb:United_States_federal_law
|
|
gptkbp:administeredBy
|
gptkb:U.S._Food_and_Drug_Administration
|
|
gptkbp:amendedBy
|
gptkb:Food_Quality_Protection_Act
gptkb:Food_and_Drug_Administration_Modernization_Act_of_1997
gptkb:Drug_Amendments_of_1962
gptkb:Medical_Device_Amendments_of_1976
|
|
gptkbp:codifiedIn
|
gptkb:Title_21_of_the_United_States_Code
|
|
gptkbp:dateEnacted
|
1938
|
|
gptkbp:enactedBy
|
gptkb:United_States_Congress
|
|
gptkbp:purpose
|
protect public health
ensure safety and efficacy of food and drugs
|
|
gptkbp:regulates
|
gptkb:food
cosmetics
drugs
medical devices
biological products
|
|
gptkbp:replacedBy
|
gptkb:Pure_Food_and_Drug_Act_of_1906
|
|
gptkbp:section
|
gptkb:Section_301_(Prohibited_Acts)
Section 351 (Adulterated Drugs and Devices)
Section 352 (Misbranded Drugs and Devices)
Section 355 (New Drugs)
Section 360 (Device Registration)
Section 374 (Inspection)
|
|
gptkbp:shortName
|
FDCA
|
|
gptkbp:title
|
gptkb:Federal_Food,_Drug,_and_Cosmetic_Act
|
|
gptkbp:bfsParent
|
gptkb:21_U.S.C._§_360bbb-3
|
|
gptkbp:bfsLayer
|
7
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
21 U.S.C. Chapter 9
|