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FDA Food contact details for thermos cups exported to the United States

Product Description

Product Description
Thermos cup can not only let you have hot water at any time, but also a winter magic device for everyone. Let's take a look at the procedures needed to export to the United States. Thermos cup is generally made of ceramic or stainless steel and vacuum layer of the container of water, the top has a cover, sealed, vacuum insulation layer can make installed in the internal water and other liquid delay heat dissipation, in order to achieve the purpose of heat preservation. The first thing you need to do when you drink something in your mouth is a food exposure test.
1. The Food and Drug Administration is the United States Food and Drug Administration.
The purpose of the FDA is to ensure the safety, hygiene, health, and proper labeling of food products in the United States and the safety and proper labeling of cosmetics;
The FDA's responsibility is to ensure the safety of food, cosmetics, drugs, biologics, medical devices, and radiological products produced or imported into the United States;
FDA is recognized as one of the largest food and drug regulatory agencies in the world;
FDA is one of the implementing agencies established by the United States Government within the Departments of Health and Human Services (DHHS) and Public Health (PHS).
2. Documents required for FDA registration:
1. Entrustment Agreement (signed by the legal representative of the applicant with the company's official seal)
2. FDA Registration Application Form (signed by the legal representative of the applicant and stamped with the official seal
Three, thermos cup for FDA testing standards:
Organic coated, Metallic and electroplated products: FDA CFR 21 175.300.
Food grade rubber: FDA 21CFR 177.2600
Iv. Procedures for FDA testing of thermos cups:
1. Consultation -- the applicant shall provide product information pictures or explain the products and materials required to apply for FDA through description;
2. Quotation -- make an assessment according to the information provided by the applicant, determine the items to be tested, and offer a quotation to the applicant;
3. Confirmation -- the applicant confirms the offer and fills in the test application form, pays, and sends the sample;
4. Testing -- testing in accordance with applicable FDA standards;
5. Completion -- FDA test report shall be provided upon completion of the test.

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