Code of Federal Regulations · Subpart

Subpart R — Laboratory Accreditation For Analyses Of Foods

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

• § 1.1101 What Documents Are Incorporated By Reference In This Subpart
• § 1.1102 What Definitions Apply To This Subpart?
• § 1.1103 Who Is Subject To This Subpart?
• § 1.1107 When Must Food Testing Be Conducted Under This Subpart?
• § 1.1108 When And How Will Fda Issue A Directed Food Laboratory Order?
• § 1.1109 How Will Fda Make Information About Recognized Accreditation Bodies And Laaf-accredited Laboratories Available To The Public?
• § 1.1110 What Are The General Requirements For Submitting Information To Fda Under This Subpart?
• § 1.1113 What Are The Eligibility Requirements For A Recognized Accreditation Body?
• § 1.1114 How Does An Accreditation Body Apply To Fda For Recognition Or Renewal Of Recognition?
• § 1.1115 How Will Fda Evaluate Applications For Recognition And Renewal Of Recognition?
• § 1.1116 What Must A Recognized Accreditation Body Do To Voluntarily Relinquish Or Not Renew Its Recognition?
• § 1.1117 How May An Accreditation Body Request Reinstatement Of Recognition?
• § 1.1119 What Are The Conflict Of Interest Requirements For A Recognized Accreditation Body?
• § 1.1120 How Must A Recognized Accreditation Body Assess Laboratories Seeking Laaf-accreditation And Oversee Laaf-accredited Laboratories?
• § 1.1121 When Must A Recognized Accreditation Body Require Corrective Action, Suspend A Laaf-accredited Laboratory, Or Reduce The Scope Of Or Withdraw The Laaf-accreditation Of A Laboratory?
• § 1.1122 What Procedures Must A Recognized Accreditation Body Provide For Appeals Of Decisions To Suspend, Reduce The Scope Of, Withdraw, Or Deny Laaf-accreditation?
• § 1.1123 What Reports, Notifications, And Documentation Must A Recognized Accreditation Body Submit To Fda?
• § 1.1124 What Are The Records Requirements For A Recognized Accreditation Body?
• § 1.1125 What Are The Internal Audit Requirements For A Recognized Accreditation Body?
• § 1.1130 How Will Fda Oversee Recognized Accreditation Bodies?
• § 1.1131 When Will Fda Require Corrective Action, Put A Recognized Accreditation Body On Probation, Or Revoke The Recognition Of An Accreditation Body?
• § 1.1138 What Are The Eligibility Requirements For A Laaf-accredited Laboratory?
• § 1.1139 How Does A Laboratory Apply For Laaf-accreditation Or Extend Its Scope Of Laaf-accreditation?
• § 1.1140 What Must A Laaf-accredited Laboratory Do To Voluntarily Relinquish Its Laaf-accreditation?
• § 1.1141 What Is The Effect On A Laaf-accredited Laboratory If Its Recognized Accreditation Body Is No Longer Recognized By Fda?
• § 1.1142 How Does A Laboratory Request Reinstatement Of Laaf-accreditation?
• § 1.1147 What Are The Impartiality And Conflict Of Interest Requirements For A Laaf-accredited Laboratory?
• § 1.1149 What Oversight Standards Apply To Sampling?
• § 1.1150 What Are The Requirements For Analysis Of Samples By A Laaf-accredited Laboratory?
• § 1.1151 What Requirements Apply To The Methods Of Analysis A Laaf-accredited Laboratory Uses To Conduct Food Testing Under This Subpart?
• § 1.1152 What Notifications, Results, Reports, And Studies Must A Laaf-accredited Laboratory Submit To Fda?
• § 1.1153 What Are The Requirements For Submitting Abridged Analytical Reports?
• § 1.1154 What Other Records Requirements Must A Laaf-accredited Laboratory Meet?
• § 1.1159 How Will Fda Oversee Laaf-accredited Laboratories?
• § 1.1160 How Will Fda Review Test Results And Analytical Reports?
• § 1.1161 When Will Fda Require Corrective Action, Put A Laaf-accredited Laboratory On Probation, Or Disqualify A Laaf-accredited Laboratory From Submitting Analytical Reports?
• § 1.1162 What Are The Consequences If Fda Puts A Laaf-accredited Laboratory On Probation Or Disqualifies A Laaf-accredited Laboratory?
• § 1.1171 How Does An Accreditation Body Request Reconsideration By Fda Of A Decision To Deny Its Application For Recognition, Renewal, Or Reinstatement?
• § 1.1173 How Does An Accreditation Body Or Laboratory Request A Regulatory Hearing On Fda's Decision To Revoke The Accreditation Body's Recognition Or Disqualify A Laaf-accredited Laboratory?
• § 1.1174 How Does An Owner Or Consignee Request A Regulatory Hearing On A Directed Food Laboratory Order?
• § 1.1199 Are Electronic Records Created Under This Subpart Subject To The Electronic Records Requirements Of Part 11 Of This Chapter?
• § 1.1200 Are The Records Obtained By Fda Under This Subpart Subject To Public Disclosure?