FDA

Question: Can someone help me understand what the is the correct FDA information to submit when importing products from a Contract manufacturer in which we are the design authority (legal manufacturer) but all manufacturing processes take place at the contract manufacturing facility in another country? My understanding is that we would use the Contract Manufacturer’s […]

Question: Is there a report we can run that will identify when we’ve been declared as the FSVP, but not the IOR? Answer 1: Currently the only way to get information on lines of entries in which you have been declared as the FSVP importer is to submit a FOIA request to FDA. We do […]

Question: My question is as it relates to the UC declared on the 7501 being subject to FSVP because we’ve had FSVP audits where we placed a domestic order and our vendor shipped directly to our US door.  As such, we were listed as the UC on our US vendor’s entry, and were flagged for […]

Question: FDA Food import requirements question – is there a way to import food samples without a Food Facility Registration number? I know Drugs and Medical Devices have a R&D intended use code you can use which does not require a manufacturer registration. Just wondering if this is also a possibility for food samples to […]

Question: Where can I find a resource that outlines each of the codes and their descriptions for industry, class, subclass, process indicator code, product, otherwise found in the FDA Product Code Builder? Answer 1: The lessons in the tutorials for the product code builder may be helpful. Here is the link: PCB Tutorial (fda.gov) Answered by: […]

Question: Under a DDP transaction, can a foreign entity (shipping food items from Europe to the US) be designated as the importer of record on an entry for customs purposes and also designated as the FSVP importer for FDA purposes? Or does there need to be a US entity declared as the FSVP importer declared? […]

Question: Recently, there was an import of perishable research samples under the FDA Memphis jurisdiction. Due to the intended use, there was no requirement to file any AOC data; only Roles information was needed. The shipment was imported, and the FDA issued a FDA Review, followed by an FDA Hold, and finally an FDA Intensive […]

Question: Hello Members: My supply chain wishes to import Non-Regulated Medical Devices for the purpose of consolidating these Non-Regulated goods with other goods and than export so as to save on transportation cost.  I don’t think I can claim TIB (9813) for the import does not qualify.   I can’t use FDA Import For Export (IFE) […]

Question: Dear Members: Does anyone know what triggers a “Manifest Hold Agriculture”?  Broker could not explain why and submitted entry docs to CBP. Also, I am seeing a good amount of FDA Holds in the Memphis area when importing under headings 3002, 3822 and 9027. At a previous company we import headings 3002, 3822 and […]

Question: Hello ICPA members.  My company is downsizing and consolidating roles.  My trade compliance function will be brought under supply chain and logistics.  It will be expanded to handle some OGA regulatory matters that are more supply chain than regulatory filings etc.  The role will involve leading the Good Distribution Practice efforts at our mfg […]

Question: Hello ICPA Community. I’m preparing to take on a role focusing on FDA Import for Exports.  Can you please recommend some resources that will help me become acquainted with the nuances of IFE?  I’m currently reading as  much as I can on the FDA site, but I’m looking for some of your tribal knowledge. […]

Question: Hello Membership!   We are brainstorming ideas to improve our export process and documentation requirements.  Do all countries require a certificate of resale from the US to import?  Is there a centralized resource available which identifies which states will issue a certificate of free sale for export and the validity of the certificate?  How do […]