On October 6, 2011, the U.S. Food and Drug Administration (FDA) announced in the Federal Register its issuance of a question-and-answer guidance document related to the implementation of the fee provisions of the Food Safety Modernization Act of 2011 (FSMA). This follows up on the August 1, 2011, publication of the fee rates for fiscal year 2012 for domestic and foreign facility reinspections, recall orders and import reinspections under the FSMA.
"The new guidance covers commonly asked questions related to the implementation of these fees under the FSMA and also provides information on the process for requesting a reduction of fees assessed in fiscal year 2012."
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