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Form Approved OMB No. 0910-0025 Expiration Date January 31 2017 FORM FDA 3630 10/14 Guide for Preparing Product Reports on Sunlamps and Sunlamp Products Public reporting burden for this collection of information is estimated to average 24 hours per response including the time for reviewing instructions searching existing data sources gathering and maintaining the data needed and completing and reviewing the collection of information. Send comment...
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What is fda form 3630?
FDA Form 3630 is a document used by the Food and Drug Administration (FDA) to collect information related to drug establishments.
Who is required to file fda form 3630?
Drug establishments and facilities that are registered with the FDA are required to file FDA Form 3630.
How to fill out fda form 3630?
To fill out FDA Form 3630, you need to provide information such as the name and address of the drug establishment, the type of drug products manufactured or distributed, and details of the responsible officials.
What is the purpose of fda form 3630?
The purpose of FDA Form 3630 is to gather information about drug establishments and ensure compliance with FDA regulations.
What information must be reported on fda form 3630?
FDA Form 3630 requires the reporting of information such as the establishment's name and address, type of drugs manufactured or distributed, and details of responsible officials.
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