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DEPARTMENT OF HEALTH AND HUMAN SERVICES FOOD AND DRUG ADMINISTRATION NAME AND LOCATION OF PLANT (Single-Service Milk Containers and Closures) MANUFACTURING PLANT INSPECTION REPORT INSPECTING AGENCY/FIRM
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FDA Form 2359c is a form used for the registration of drug establishments and listing of drugs with the U.S. Food and Drug Administration (FDA).
All domestic and foreign drug establishments that engage in the manufacturing, repacking, or relabeling of drugs for commercial distribution in the United States are required to file FDA Form 2359c.
To fill out FDA Form 2359c, the establishment must provide information about the facility, location, ownership, activities, drug products, and contact details. The form can be filled out electronically through the FDA's registration and listing system.
The purpose of FDA Form 2359c is to ensure proper registration and listing of drug establishments and their products with the FDA. It helps the FDA track and monitor drug manufacturing, distribution, and safety.
FDA Form 2359c requires the reporting of various information including establishment details, drug product information, manufacturing activities, labeling, drug codes, and contact information. The specific details required can be found in the form's instructions.
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