Professional Documents
Culture Documents
Contents
Subpart A—General Provisions
§1.1 General.
§1.3 Definitions.
§1.4 Authority citations.
§1.70 Scope.
§1.71 Definitions.
§1.72 Data elements that must be submitted in ACE for articles regulated by FDA.
§1.73 Food.
§1.74 Human drugs.
§1.75 Animal drugs.
§1.76 Medical devices.
§1.77 Radiation-emitting electronic products.
§1.78 Biological products, HCT/Ps, and related drugs and medical devices.
§1.79 Tobacco products.
§1.80 Cosmetics.
§1.81 Rejection of entry filing.
Subpart E—Imports and Exports
§1.83 Definitions.
§1.90 Notice of sampling.
§1.91 Payment for samples.
§1.94 Hearing on refusal of admission or destruction.
§1.95 Application for authorization to relabel and recondition.
§1.96 Granting of authorization to relabel and recondition.
§1.97 Bonds.
§1.99 Costs chargeable in connection with relabeling and reconditioning inadmissible imports.
§1.101 Notification and recordkeeping.
Subparts F-G [Reserved]
GENERAL PROVISIONS
§1.352 What information must transporters establish and maintain?
GENERAL REQUIREMENTS
GENERAL PROVISIONS
Subpart M—Accreditation of Third-Party Certification Bodies To Conduct Food Safety Audits and To Issue
Certifications