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FDA to Reject Entry Data When It Contradicts with the Entry Type

Home News FDA to Reject Entry Data When It Contradicts with the Entry Type

FDA to Reject Entry Data When It Contradicts with the Entry Type

U.S. Food and Drug Administration (FDA) validations will be updated to enforce the PGA Flag Enforcement table. If FDA receives an entry with the FDA message set on an entry type not subject to FDA import requirements, FDA will reject the entry data with subreason code 195, Entry Type Not Allowed for PGA.

Specifically, if trade submits an Entry Type 22 with FDA data, the entry data will be rejected by FDA for correction of the conflicting information.

Note: Entry Types 31, 32, 34 and 38 are valid for Entry Summary. FDA data is processed on cargo release transactions.

This enhancement was deployed in the lower environment for testing on December 17, 2021. Testing is encouraged. This production deployment has been changed to January 22, 2022 at approximately 11PM.

For questions regarding this reject or FDA ACE technical inquiries, contact FDA ACE Support, ACE_Support@fda.hhs.gov. ACE Support Hours: Monday – Friday, 8:00 AM – 8:00 PM.

Notice can be found here.

Source: U.S. Customs and Border Protection (CBP)

About CBP: With more than 60,000 employees, U.S. Customs and Border Protection, CBP, is one of the world’s largest law enforcement organizations and is charged with keeping terrorists and their weapons out of the U.S. while facilitating lawful international travel and trade. As the United States’ first unified border entity, CBP takes a comprehensive approach to border management and control, combining customs, immigration, border security, and agricultural protection into one coordinated and supportive activity.

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