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Form Approved: OMB No. 09100025 Expiration Date: August 31, 2023FORM FDA 3627 (09/20) A Guide for the Submission of Initial Reports on Computed Tomography Ray SystemsPublic reporting burden for this
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What is form fda 3627 0920?
FDA Form 3627 0920 is a form used for reporting of product information for human prescription drugs.
Who is required to file form fda 3627 0920?
Manufacturers, packers, and distributors of human prescription drugs are required to file form FDA 3627 0920.
How to fill out form fda 3627 0920?
Form FDA 3627 0920 can be filled out electronically through the FDA's Electronic Submissions Gateway (ESG) or manually by printing out the form and completing it with the required information.
What is the purpose of form fda 3627 0920?
The purpose of form FDA 3627 0920 is to report product information for human prescription drugs to the FDA.
What information must be reported on form fda 3627 0920?
Form FDA 3627 0920 requires reporting of product labeling, packaging information, and any changes made to the product.
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