CFR /  Title 21  /  Part 1: General Enforcement Regulations

Section No.	Description
Section 1.1	Definitions
Section 1.3	Authority citations
Section 1.4	Presence of mandatory label information
Section 1.20	Failure to reveal material facts
Section 1.21	Procedures for requesting variations and exemptions from required label statements
Section 1.23	Exemptions from required label statements
Section 1.24	Definitions
Section 1.83	Notice of sampling
Section 1.90	Payment for samples
Section 1.91	Hearing on refusal of admission
Section 1.94	Application for authorization to relabel and recondition
Section 1.95	Granting of authorization to relabel and recondition
Section 1.96	Bonds
Section 1.97	Costs chargeable in connection with relabeling and reconditioning inadmissible imports
Section 1.99	Notification and recordkeeping
Section 1.101	Who must register under this subpart?
Section 1.225	Who does not have to register under this subpart?
Section 1.226	What definitions apply to this subpart?
Section 1.227	When must you register?
Section 1.230	How and where do you register?
Section 1.231	What information is required in the registration?
Section 1.232	What optional items are included in the registration form?
Section 1.233	How and when do you update your facility's registration information?
Section 1.234	How and when do you cancel your facility's registration information?
Section 1.235	What other registration requirements apply?
Section 1.240	What are the consequences of failing to register, update, or cancel your registration?
Section 1.241	What does assignment of a registration number mean?
Section 1.242	Is food registration information available to the public?
Section 1.243	What definitions apply to this subpart?
Section 1.276	What is the scope of this subpart?
Section 1.277	Who is authorized to submit prior notice?
Section 1.278	When must prior notice be submitted to FDA?
Section 1.279	How must you submit prior notice?
Section 1.280	What information must be in a prior notice?
Section 1.281	What must you do if information changes after you have received confirmation of a prior notice from FDA?
Section 1.282	What happens to food that is imported or offered for import without adequate prior notice?
Section 1.283	What are the other consequences of failing to submit adequate prior notice or otherwise failing to comply with this
Section 1.284	What happens to food that is imported or offered for import from unregistered facilities that are required to register
Section 1.285	Who is subject to this subpart?
Section 1.326	Who is excluded from all or part of the regulations in this subpart?
Section 1.327	What definitions apply to this subpart?
Section 1.328	Do other statutory provisions and regulations apply?
Section 1.329	Can existing records satisfy the requirements of this subpart?
Section 1.330	What information must nontransporters establish and maintain to identify the nontransporter and transporter immediate
Section 1.337	What information must nontransporters establish and maintain to identify the nontransporter and transporter immediate
Section 1.345	What information must transporters establish and maintain?
Section 1.352	What are the record retention requirements?
Section 1.360	What are the record availability requirements?
Section 1.361	What records are excluded from this subpart?
Section 1.362	What are the consequences of failing to establish or maintain records or make them available to FDA as required by
Section 1.363	What are the compliance dates for this subpart?
Section 1.368	What definitions apply to this subpart?
Section 1.377	What criteria does FDA use to order a detention?
Section 1.378	How long may FDA detain an article of food?
Section 1.379	Where and under what conditions must the detained article of food be held?
Section 1.380	May a detained article of food be delivered to another entity or transferred to another location?
Section 1.381	What labeling or marking requirements apply to a detained article of food?
Section 1.382	What expedited procedures apply when FDA initiates a seizure action against a detained perishable food?
Section 1.383	When does a detention order terminate?
Section 1.384	Who approves a detention order?
Section 1.391	Who receives a copy of the detention order?
Section 1.392	What information must FDA include in the detention order?
Section 1.393	Who is entitled to appeal?
Section 1.401	What are the requirements for submitting an appeal?
Section 1.402	What requirements apply to an informal hearing?
Section 1.403	Who serves as the presiding officer for an appeal, and for an informal hearing?
Section 1.404	When does FDA have to issue a decision on an appeal?
Section 1.405	How will FDA handle classified information in an informal hearing?
Section 1.406	Administrative detention of drugs
Section 1.980	Imminent hazard to the public health