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Requirements for User Fees Under This Subpart
Law
CFR 21
Food and Drugs
Food and Drug Administration, Department of Health and Human Services
General
General Enforcement Regulations
Accreditation of Third-Party Certification Bodies To Conduct Food Safety Audits and To Issue Certifications
Requirements for User Fees Under This Subpart
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Section
1.700
Who is subject to a user fee under this subpart?
Section
1.705
What user fees are established under this subpart?
Section
1.710
How will FDA notify the public about the fee schedule?
Section
1.715
When must a user fee required by this subpart be submitted?
Section
1.720
Are user fees under this subpart refundable?
Section
1.725
What are the consequences of not paying a user fee under this subpart on time?