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04-1779 OGA-CBP FDA ADDITIONAL EDITS AND VALIDATIONS AUGUST 13, 2004, ADMINISTRATIVE MESSAGE 04-1779 08/10/2004 TITLE: OGA-CBP FDA ADDITIONAL EDITS AND VALIDATIONS AUGUST 13, 2004, ATTENTION ALL ABI
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What is 04-1779 oga-cbp fda additional?
04-1779 oga-cbp fda additional refers to a specific form used to report additional information related to the importation of goods regulated by the U.S. Food and Drug Administration (FDA) through the Office of Regulatory Affairs (ORA). It is typically used when there are certain requirements or issues that need to be addressed beyond the standard import procedures.
Who is required to file 04-1779 oga-cbp fda additional?
Importers or their authorized agents are generally required to file the 04-1779 oga-cbp fda additional form when they are importing goods that fall under the regulation of the FDA. This includes food, drugs, medical devices, cosmetics, and other products subject to FDA oversight.
How to fill out 04-1779 oga-cbp fda additional?
To fill out the 04-1779 oga-cbp fda additional form, importers or their authorized agents must provide detailed information about the imported goods, including product descriptions, quantities, country of origin, intended use, and FDA-related information. It is important to accurately complete all required fields and provide any necessary supporting documentation.
What is the purpose of 04-1779 oga-cbp fda additional?
The purpose of the 04-1779 oga-cbp fda additional form is to ensure compliance with FDA regulations and to provide the necessary information for the FDA to assess the safety, quality, and proper labeling of imported products. It helps facilitate appropriate oversight and evaluation of imported goods to protect public health.
What information must be reported on 04-1779 oga-cbp fda additional?
The specific information required to be reported on the 04-1779 oga-cbp fda additional form may vary depending on the nature of the imported goods and the requirements of the FDA. However, common information that may need to be reported includes product descriptions, quantities, country of origin, intended use, labeling information, and FDA-related data such as registration numbers or prior notices.
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