Code of Federal Regulations · Subpart

Subpart M — Accreditation Of Third-party Certification Bodies To Conduct Food Safety Audits And To Issue Certifications

21 C.F.R. pt. 1, subpt. M

• § 1.600 What Definitions Apply To This Subpart?
• § 1.601 Who Is Subject To This Subpart?
• § 1.610 Who Is Eligible To Seek Recognition?
• § 1.611 What Legal Authority Must An Accreditation Body Have To Qualify For Recognition?
• § 1.612 What Competency And Capacity Must An Accreditation Body Have To Qualify For Recognition?
• § 1.613 What Protections Against Conflicts Of Interest Must An Accreditation Body Have To Qualify For Recognition?
• § 1.614 What Quality Assurance Procedures Must An Accreditation Body Have To Qualify For Recognition?
• § 1.615 What Records Procedures Must An Accreditation Body Have To Qualify For Recognition?
• § 1.620 How Must A Recognized Accreditation Body Evaluate Third-party Certification Bodies Seeking Accreditation?
• § 1.621 How Must A Recognized Accreditation Body Monitor The Performance Of Third-party Certification Bodies It Accredited?
• § 1.622 How Must A Recognized Accreditation Body Monitor Its Own Performance?
• § 1.623 What Reports And Notifications Must A Recognized Accreditation Body Submit To Fda?
• § 1.624 How Must A Recognized Accreditation Body Protect Against Conflicts Of Interest?
• § 1.625 What Records Requirements Must An Accreditation Body That Has Been Recognized Meet?
• § 1.630 How Do I Apply To Fda For Recognition Or Renewal Of Recognition?
• § 1.631 How Will Fda Review My Application For Recognition Or Renewal Of Recognition And What Happens Once Fda Decides On My Application?
• § 1.632 What Is The Duration Of Recognition?
• § 1.633 How Will Fda Monitor Recognized Accreditation Bodies?
• § 1.634 When Will Fda Revoke Recognition?
• § 1.635 What If I Want To Voluntarily Relinquish Recognition Or Do Not Want To Renew Recognition?
• § 1.636 How Do I Request Reinstatement Of Recognition?
• § 1.640 Who Is Eligible To Seek Accreditation?
• § 1.641 What Legal Authority Must A Third-party Certification Body Have To Qualify For Accreditation?
• § 1.642 What Competency And Capacity Must A Third-party Certification Body Have To Qualify For Accreditation?
• § 1.643 What Protections Against Conflicts Of Interest Must A Third-party Certification Body Have To Qualify For Accreditation?
• § 1.644 What Quality Assurance Procedures Must A Third-party Certification Body Have To Qualify For Accreditation?
• § 1.645 What Records Procedures Must A Third-party Certification Body Have To Qualify For Accreditation?
• § 1.650 How Must An Accredited Third-party Certification Body Ensure Its Audit Agents Are Competent And Objective?
• § 1.651 How Must An Accredited Third-party Certification Body Conduct A Food Safety Audit Of An Eligible Entity?
• § 1.652 What Must An Accredited Third-party Certification Body Include In Food Safety Audit Reports?
• § 1.653 What Must An Accredited Third-party Certification Body Do When Issuing Food Or Facility Certifications?
• § 1.654 When Must An Accredited Third-party Certification Body Monitor An Eligible Entity That It Has Issued A Food Or Facility Certification?
• § 1.655 How Must An Accredited Third-party Certification Body Monitor Its Own Performance?
• § 1.656 What Reports And Notifications Must An Accredited Third-party Certification Body Submit?
• § 1.657 How Must An Accredited Third-party Certification Body Protect Against Conflicts Of Interest?
• § 1.658 What Records Requirements Must A Third-party Certification Body That Has Been Accredited Meet?
• § 1.660 Where Do I Apply For Accreditation Or Renewal Of Accreditation By A Recognized Accreditation Body And What Happens Once The Recognized Accreditation Body Decides On My Application?
• § 1.661 What Is The Duration Of Accreditation By A Recognized Accreditation Body?
• § 1.662 How Will Fda Monitor Accredited Third-party Certification Bodies?
• § 1.663 How Do I Request An Fda Waiver Or Waiver Extension For The 13-month Limit For Audit Agents Conducting Regulatory Audits?
• § 1.664 When Would Fda Withdraw Accreditation?
• § 1.665 What If I Want To Voluntarily Relinquish Accreditation Or Do Not Want To Renew Accreditation?
• § 1.666 How Do I Request Reaccreditation?
• § 1.670 How Do I Apply To Fda For Direct Accreditation Or Renewal Of Direct Accreditation?
• § 1.671 How Will Fda Review My Application For Direct Accreditation Or Renewal Of Direct Accreditation And What Happens Once Fda Decides On My Application?
• § 1.672 What Is The Duration Of Direct Accreditation?
• § 1.680 How And When Will Fda Monitor Eligible Entities?
• § 1.681 How Frequently Must Eligible Entities Be Recertified?
• § 1.690 How Will Fda Make Information About Recognized Accreditation Bodies And Accredited Third-party Certification Bodies Available To The Public?
• § 1.691 How Do I Request Reconsideration Of A Denial By Fda Of An Application Or A Waiver Request?
• § 1.692 How Do I Request Internal Agency Review Of A Denial Of An Application Or Waiver Request Upon Reconsideration?
• § 1.693 How Do I Request A Regulatory Hearing On A Revocation Of Recognition Or Withdrawal Of Accreditation?
• § 1.694 Are Electronic Records Created Under This Subpart Subject To The Electronic Records Requirements Of Part 11 Of This Chapter?
• § 1.695 Are The Records Obtained By Fda Under This Subpart Subject To Public Disclosure?
• § 1.700 Who Is Subject To A User Fee Under This Subpart?
• § 1.705 What User Fees Are Established Under This Subpart?
• § 1.710 How Will Fda Notify The Public About The Fee Schedule?
• § 1.715 When Must A User Fee Required By This Subpart Be Submitted?
• § 1.720 Are User Fees Under This Subpart Refundable?
• § 1.725 What Are The Consequences Of Not Paying A User Fee Under This Subpart On Time?