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FDA FSVP Inspection Support

We help importers prepare for and respond to FDA FSVP inspections, with mock inspections, documentation review, and corrective action support built around your supplier records. We work with clients based in Florida, across the United States, and internationally.

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Ready Before FDA Reviews Your FSVP Records

An FSVP inspection looks closely at how well your supplier verification records hold up, not just whether they exist. We help you prepare those records, run a practice inspection to catch gaps early, and stay by your side if FDA raises questions during or after the review. Browse the services below, or reach out and we’ll assess where your FSVP program currently stands.
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FDA FSVP Inspection Support

Prepare for and respond to FDA FSVP inspections, with mock inspections, documentation review, and corrective action support.
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FSVP Inspection Preparation

Get your FSVP records, supplier files, and verification documentation organized and ready before FDA arrives. We walk through what an investigator typically reviews so nothing catches your team off guard.

FSVP Documentation Review

Review your existing FSVP records for completeness and accuracy against current FDA requirements. This catches outdated or missing supplier documentation before an inspector does.

Mock FSVP Inspections

Run a practice inspection that mirrors what FDA actually looks for during an FSVP review. This surfaces gaps early enough to fix them before the real inspection happens.

Ongoing FSVP Compliance Management

Keep your FSVP program current between inspections, with regular reviews and updates as your supplier list changes. This keeps you inspection-ready year-round instead of scrambling before a visit.

FDA FSVP Inspection Support

Provide direct, on-the-day support while FDA conducts an FSVP inspection at your facility. We help make sure your team can answer questions and produce records without unnecessary delays.

FDA FSVP Response Assistance

Help you respond to FDA's questions and findings during and after an FSVP inspection. This includes drafting written responses and supporting documentation.

FSVP Corrective Action Development & Implementation

Build and put into place the corrective actions needed to resolve issues found during an FSVP inspection. We help make sure the fix addresses the root cause, not just the immediate observation.
Faq

Frequently Asked Questions

During an FSVP inspection, FDA reviews your supplier verification records, hazard analysis reviews, and documentation to confirm your program meets requirements. Investigators may also ask your team questions about how the verification process actually works day to day.
A mock FSVP inspection is a practice run that mirrors what FDA looks for during a real inspection, using your actual records and supplier files. It helps identify gaps while there is still time to fix them, rather than during the real inspection.

Yes. We work with importers based in Florida as well as companies across the United States and internationally.

A shipment can be placed on hold if FDA or customs identifies a documentation gap or compliance concern, and it generally cannot proceed until the issue is resolved. We help importers respond quickly with the documentation or corrective action needed to release the shipment.

Prior notice is advance notification to FDA about a food shipment before it arrives in the United States, required for nearly all imported food shipments. Missing or incorrect prior notice is one of the most common reasons a shipment gets held.

Yes. We coordinate documentation between your foreign suppliers and your customs broker so entry filings and supporting records stay consistent and complete.

A nonconforming shipment does not meet FDA or customs requirements, whether due to a documentation issue or a product-level compliance problem. Handling it correctly requires specific documentation and corrective steps, which we help importers prepare.

Yes. We help manage the documentation and process for claims tied to damaged, rejected, or noncompliant shipments, so importers can pursue recovery while keeping their records clean.