Snow: 18768899273
Tel
15517851322
WP

7*24 hours service hotline

15517851322

Scan to add Us

Snow
Pinkeman Intellectual Property Consultants

Trademark registration, patent application Industry consultant, senior experience, platform guarantee, follow-up

PINKEMAN IP service ~~
Location: Home > Blog > AMZ Knowledge

What is COA certification?How to do Amazon COA certification

发布日期:2022-08-26  浏览次数:   信息来源:小编

COA is a customs clearance certificate. After the product enters the customs, the importer can apply for the MS label from Sirim by virtue of COA. Special, if you want to directly add a logo in the factory, you need to apply for Sirim's inspection factory. Because of the high cost, this method is generally aimed at manufacturers with high frequency of shipments.

Application process
If the customer does not test the report, it needs to be tested
. Customers prepare information and apply to submit to UEST
3. UEST submits the information to the agent, and the agent is submitted to the institution ST
4. ST audit document, issue certificate
5. Importers purchase labels from Sirim

certification sign
ST COA certification, there are two main types, one is Sirim Label, and the other It is Sirim Certification Mark. Note that all tags must be pasted on the product itself, and cannot be pasted on the packaging.

Other information
Technical information: voltage frequency AC 240V, 50Hz, plug MS 589 / BS 1363 / ms 1577 / bs 546 / ms 1578 / bs EN 50075
Whether forced: mandatory [123 123 ] Certificate Validity: One year Effective
Factory requirements: Generally speaking, there is no requirement. If you apply for a certification label in the factory, you need to accept the inspection factory
The request of the holder: must be a local registered importer

The COA certificate is valid for one year, and the applicant needs to end at the validity period of the certificate validity period. The COA update is completed 14 days before the date. The label must be purchased according to the actual import volume of the product or the production volume and Sirim.

\u0026#8212; \u0026#8212; \u0026#8212; \u0026#8212; \u0026#8212; \u0026#8212; \u0026#8212; \u0026#8212; \u0026#8212;-

COA, Certification of Analysis, product inspection certificate, if the customer does not specify third -party certification, your factory will issue an official seal for themselves, and most customers need to use this thing when importing customs clearance.

Regarding the specific content of COA, it must be determined according to the nature of your company's product and customer requirements. For example, we are doing iron alloys, so this CoA is written on the content of each element in the product, which is very simple. As long as you write according to the characteristics of your product, write the main parameters of the product (that is, the parameters that the customer cares more)Just go up. It's OK to make a form, it is easy to do ~

\u0026#8212; \u0026#8212; \u0026#8212; \u0026#8212; \u0026#8212; \u0026#8212; \u0026 #8212; \u0026#8212; \u0026#8212; \u0026#8212; \u0026#8212;

Certificate of autors, also known as genuine certification tags or anti -counterfeiting certificates. Prove (coa) label. It can be said that it is a significant sign of identifying Microsoft genuine software products. If the genuine certification label is missing, it indicates that you may not have a genuine Windows operating system software.

Analysis report

Certificate of Analysis (mostly chemical) analysis report. The quality test report COA is the quality inspection of the product before the product. Written proof of quality standards. It is obtained by the quality inspection of the product and equipment, and it is the standard for ensuring the product quality system.

US FDA certification

US Food and Drug Administration [1] Food and Drug Administration abbreviation), belongs to the US Department of Health Education and Welfare, is responsible for national drugs, food, biological products, cosmetics, and cosmetics, and Management of veterinary drugs, medical equipment and diagnostic supplies.

The preliminary inspection of imported products is a record review.

By recording and reviewing cosmetics, one of the following three decisions will be made:

1. This batch is released

2. This batch is automatically detained

3. Through the dock inspection or sampling for inspection

For cosmetics, the dock inspection basically includes label inspection for mandatory labels to determine whether the cosmetics label is contained or listed the following content :

ingredient labels, disable ingredients, English labels, pigments that are not allowed to be used, warning instructions required by regulations, and products that need to be anti -interference required for section 21CFR700.25.

Other compulsory label information:

If the name and address of the manufacturer factory, the name and address of the packaging dealer or dealer company, the name of the content of the content, the content of the content of the content and the net content of the content.

Inspectors who conducted imported inspections can conduct a dock inspection or draw samples for all inbound products, multiple batches or single series of products. The sampling generally includes the physical collection or file summary of the product, which is used in the subsequent inspection of the Laboratory of the FDA area. Whenever the FDA draws the sample, the sample will always be the owner or the underwriterProvide a sampling notice. Tests can include pigment analysis, dirt analysis, microbial analysis, or chemical pollution analysis. The inspection is also a review label or label production to determine whether the requirements of the label production of cosmetics or whether there is a curative effect or a drug statement.

Import procedures are as follows:

In the 5 working days from the date of arriving in the goods, importers or institutions fill in the US Customs General Administration. When the FDA receives an entry notice , Review the customs declaration unit of the importer to determine whether to conduct a physical inspection (dock test, sampling test). If the sample is decided not to draw the sample, the FDA will be sent to the US customs and the case and the importer (non -notice). At this time, the goods of this batch are released at the FDA. Note that \u0026#8221; may not continue to renew \u0026#8221; does not mean that the product meets the requirements. It only means that the FDA does not test when the product enters. If the product is discovered in the future, the product violates laws and regulations, and will start the corresponding legal measures (such as confiscation, etc.) depending on the nature of illegal nature. If the sampling is decided, the FDA will send the US customs and cases and importers. ; The batch of goods must be kept in the same way, and the FDA will draw samples from the batch of goods.