Customs City Blog

eManifest & Customs Compliance News

All products regulated by the FDA have to be submitted to a review FDA before being allowed into the United States. The FDA employs an electronic review process of all submissions for entry via the Customs and Border Protection Agency (CBP). All products that are regulated by the FDA
Customs City’s Type 86 and ACE Air Customs Compliance System helps Sung Moo Kim CHB to Streamline Their Customs Compliance processes for high-volume US Section 321 eCommerce Shipments and Save More than 40% in Costs and Manual Tasks Summary   Client: Sung Moo Kim CHB Challenge: To streamline and
Since the CBP requires importers to submit electronic documentation through the Automated Broker Interface, (ABI) importers need to have access to software that connects to CBP. ABI software makes it possible to file Partner Government Agency (PGA) documentation, entries, and entry summaries and can also be useful for querying
Entry Type 86 is a voluntary entry type for the filing and electronic release of eCommerce shipments that qualify under CBP’s de minimis (<= $800 USD).  Shipments qualifying under the CBP de mimimis are also known as Section 321 shipments. Type 86 entries have to be filed by a
In-bond shipments and the reporting of the export and arrival of in-bond shipments have to be sent to CBP electronically. In the past, it was possible to submit a paper copy of the 7512 to CBP and then get the CBP officer to close the in-bond. What is the
The United States Customs & Border Protection Agency (CBP) deployed a test of a new informal type of entry on September 28, 2019. The new entry known as “Type 86” covers entry for low-value Section 321 shipments. According to CBP, the entry type is expected to enhance security and