Food Safety Modernization Act Domestic and Foreign Facility Reinspection, Recall, and Importer Reinspection Fee Rates for Fiscal Year 2027
Published Date: 7/30/2026
Notice
Summary
The Food and Drug Administration (FDA or we) is announcing the fiscal year (FY) 2027 fee rates for certain domestic and foreign facility reinspections, failures to comply with a recall order, and importer reinspections that are authorized by the Federal Food, Drug, and Cosmetic Act (FD&C Act), as amended by the FDA Food Safety Modernization Act (FSMA).
Analyzed Economic Effects
4 provisions identified: 1 benefits, 3 costs, 0 mixed.
FY2027 FSMA Hourly Fee Rates
For FY2027, FDA set the hourly rates used to bill for reinspections and related activities at $354 per hour when domestic travel is required and $414 per hour when foreign travel is required. These rates apply from October 1, 2026 through September 30, 2027 and will be used to calculate fees billed to responsible parties, U.S. agents, and importers.
Who Triggers FSMA Fees
FDA will assess fees when: (1) a domestic or foreign facility is reinspected after an initial inspection had a final classification of Official Action Indicated (OAI) for noncompliance materially related to food safety, and (2) an importer or responsible party fails to comply with a recall order. Fees are billed based on the number of direct hours spent on the reinspection or recall-related activities, charged at the hourly rates in the FY2027 fee schedule.
Payment Terms and Collections
FDA will send an invoice after it completes the billed work and payments must be made within 30 days of the invoice date in U.S. currency by electronic check (ACH/eCheck), credit card, or wire transfer. Credit card payments are only accepted for balances under $25,000; unpaid fees will be treated as a U.S. Government claim and may be referred to collections.
Small Business Fee Reduction Consideration
FDA says it recognizes that full cost recovery could impose severe hardship on small businesses and intends to consider reducing certain fees for those firms. FDA also states it does not intend to issue invoices for reinspection or recall order fees until it publishes separate guidance describing how firms may request a fee reduction.
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Key Dates
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