Mistake 1: Wrong HTS code
The Harmonized Tariff Schedule code drives classification, duty, and which agency rules apply. A wrong code can send a food or supplement entry down the wrong path, trigger a mismatch with FDA records, or invite a re-classification review.
Fix: Confirm the code against the actual product and intended use before the broker files. When in doubt, get a binding picture from the product specification rather than guessing from a similar item.
Mistake 2: Missing or late Prior Notice
Prior Notice is required for most food and supplement entries, and it must be filed within a set window before arrival. A missing or mismatched notice means FDA cannot match the shipment, which can hold the line immediately.
Fix: Fichier Avis préalable with data that matches the entry exactly, and time it to the real arrival estimate rather than the booking date.
Mistake 3: Label does not meet FDA rules
Labels are a top reason for holds. Missing nutrition facts, wrong serving sizes, unallowed claims, or missing manufacturer details all create a compliance gap that FDA can act on at the border.
Fix: Pre-review every étiquette du complément alimentaire and food label against current FDA format and claim rules before production finishes, not after the goods are boxed.
Mistake 4: No certificate of analysis
Without a certificate of analysis (COA), the importer cannot show the product meets contaminant and identity specs. If FDA asks during an exam, the missing COA becomes the reason for a hold or detention.
Fix: Require a COA per batch from the supplier and keep it with the shipment file. The Liste de contrôle des documents d'importation des ingrédients shows where the COA fits in the full set.
Mistake 5: FSVP not in place
The Foreign Supplier Verification Program is the importer’s obligation, and FDA can ask for it during clearance. Importers who assume the forwarder or broker covers it find themselves without the required verification records.
Fix: Stand up the Importateur FSVP program before the first shipment, with supplier approval and monitoring documented.
Mistake 6: Ingredients not reviewed
An unnotified new dietary ingredient, a prohibited substance, or a claim-driving component can sink an entire entry. Ingredient review is often skipped in the rush to launch a product.
Fix: Review the formulation against FDA permissibility before sourcing. This step also reduces the risk of landing on an Alerte à l'importation de la FDA later.
Mistake 7: Documents do not match the product
The invoice, packing list, label copy, and physical product must describe the same thing. A mismatch, even a small one, raises a red flag and can escalate into a full exam or refusal.
Fix: Reconcile all documents against the actual goods before departure. Consistency across papers is one of the cheapest forms of risk control.
Pulling it together
None of these seven errors is hard to avoid once it is on your radar. They all share the same root: regulatory work left until the border. The Importations en provenance de Chine vers les États-Unis, selon la FDA process is manageable when each step is owned before sailing.
These mistakes also explain most holds in our Autorisation de la FDA vs autorisation standard comparison, and they extend the timing risks covered in the Délais d'autorisation de la FDA. Close them early and the whole entry moves faster.
Foire aux questions
What is the most common FDA clearance mistake?
Missing or late Prior Notice is among the most frequent, because it stops FDA from matching the shipment. Wrong HTS codes and label errors are close behind as repeat causes of holds.
Can a wrong HTS code cause a hold?
Yes. A wrong code can mismatch FDA records, change which rules apply, or trigger a reclassification review. The hold may not be immediate, but the error surfaces during clearance.
Do I really need a certificate of analysis?
For most food and supplement entries, yes. The COA shows the product meets identity and contaminant specs, and its absence weakens your position during an FDA exam.
Is FSVP the broker’s responsibility?
No. The Foreign Supplier Verification Program is the importer of record’s obligation. The broker may file a reference, but the importer must hold the underlying records.
How do I avoid an import alert on my supplements?
Review ingredients before sourcing, keep claims within allowed language, demand certificates of analysis, and screen suppliers against the alert list. Prevention upstream is the only reliable defense.
Why must documents match the product exactly?
Any mismatch between the invoice, packing list, label, and physical goods raises a red flag that can escalate into an exam or refusal. Consistency across papers is cheap insurance against holds.
Key takeaways
Seven mistakes account for most FDA holds on food and supplement imports: wrong HTS code, missing Prior Notice, bad labels, no COA, no FSVP, unreviewed ingredients, and document mismatch. Each has a simple fix applied before the vessel sails. Build the checks into your pre-shipment routine and the border becomes a formality. The FDA food labeling guidance is the reference to keep open while you review labels.