FSVP Audit Support

What Happens During an FSVP Audit?

The FDA may inspect your Foreign Supplier Verification Program (FSVP) records for several reasons: a routine check, a past compliance issue, or because your imported product is linked to a recall. No matter the reason, being unprepared isn’t an option.

Once contacted, your FSVP manager (or designated agent) must be ready to provide all required documentation, often within 24 hours. These documents can sometimes be submitted electronically, but they must be complete, accurate, and in English. During the audit, the FDA investigator will:

  • Ask questions about your FSVP program
  • Review documentation
  • Request translated copies of key records
  • Conduct an exit interview to share observations or request corrective actions

How Sirocco Can Help

  • We offer flexible FSVP audit support, including:
  • Acting as your official U.S. FSVP agent
  • Helping your in-house FSVP representative prepare and organize documentation
  • Reviewing and improving your FSVP plan before submission
  • Offering post-audit support to address corrective actions

Whether you’re facing an FDA inspection or simply want peace of mind, our expert team is here to make sure you’re audit-ready with clarity, speed, and confidence.

Why Work With Us?

  • Over 20 years of food safety and regulatory expertise
  • Hands-on experience with CFIA audits across multiple sectors
  • Transparent pricing and no-fluff consulting
  • Proven track record helping clients gain and maintain compliance

Sirocco Consulting is trusted by food manufacturers, importers, and distributors across Canada who value expert support without the red tape.

Let us handle the compliance, so you can focus on your business. Book a Consultation Today.

Not sure what to expect from the FDA?

Get a sample FSVP audit letter and know exactly how to prepare.

What Clients Are Saying

Select your currency
USD United States (US) dollar