FDA 483 - Virbac AH, Inc - September 12, 2025

An FDA Form 483 was issued to Virbac AH, Inc in Westlake, TX, following an inspection of their Foreign Supplier Verification Program (FSVP). The inspection revealed two observations related to inadequate documentation of hazard analysis reviews for foreign suppliers and failure to provide the FSVP importer's email address during U.S. Customs and Border Protection entry filings. These issues indicate deficiencies in the firm's compliance with FSVP requirements.