Data Structure ?
147M
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、違反商品を市場から撤去すること、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、個人または会社に対して違反通知状を発出することや、個人または会社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、違反行為に対して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されます。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件に対して自発的なリコールが2件しかない。これは食品や医療機器にも当てはまるのだろうか？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な特別な要素があるのだろうか？[1]: https://open.fda.gov/downloads/
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