Compliance Audits & Reviews
Structured reviews to identify gaps and strengthen your FSVP before FDA does
We conduct focused internal reviews of your FSVP documentation to identify missing elements, outdated records, or gaps in verification activities. These assessments help importers confirm that their program aligns with FDA expectations and is ready for record requests or inspections.
What’s included
- Mock FSVP inspections
- Review of FSVP records, supplier documentation and verification activities
- Identification of incomplete, outdated, or missing records
- Review of hazard analyses and supplier evaluations
- Corrective-action recommendations
- Follow-up guidance to support documentation updates
- Gap summaries outlining what needs to be corrected and how
Deliverables You Receive
- A summary with all review findings and program evaluation
- A clear list of required updates or corrections
- Written gap assessment report
- Corrective-action recommendations with practical next steps
- Review notes aligned with FSVP requirements
- Strengthened documentation ahead of FDA interaction
How This Supports Compliance
Conducting routine internal reviews helps catch issues before FDA does. Regular audits ensure your FSVP remains complete, current, and aligned with the requirements for supplier verification, documentation, and risk evaluation.
Request a Quote
We’ll review your category-specific FSVP requirements and return a detailed proposal.