Data Structure ?
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Data Structure ?
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README.md
FDAの規制計画の目標は、『連邦食品医薬品化粧品法』（法と略称）の遵守を確保することです。具体的な執法活動には、違反行為の是正と予防、市場から違反製品や商品を撤去すること、および違反者の処罰が含まれます。FDAが行う執法活動の種類は、違反行為の性質によって異なります。執法活動の範囲には、個人または企業に違反通知状を発出すること、および個人または企業に対する刑事訴追を求めることが含まれます。偽装または誤った表示は、通常、個人が法律の遵守を確保するための措置を講じなかった結果です。このような個人は、違反行為に責任を負う可能性があり、有罪判決を受けた場合、法律で定められた罰則が科せられます。米国食品医薬品局（FDA）がこのデータセットを提供してくれたことに感謝します。あなたはここで[データセットの最新バージョン][1]を見つけることができます。啓示——麻薬取締り行動1000件につき、自主的なリコールはわずか2件です。これは食品や医療機器にも当てはまるでしょうか？非自発的な執法行動には、業界が基本的に自己規制を行うようにする特別な理由はありますか？[1]: https://open.fda.gov/downloads/
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- 1. The data originates from internet data collection or provided by service providers, and this platform offers users the ability to view and browse datasets.
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- 3. Basic dataset information comes from the original data source or the information provided by the data provider. If there are discrepancies in the dataset description, please refer to the original data source or service provider's address.
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