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Electronic Code of Federal Regulations

blue pill

e-CFR Data is current as of July 28, 2014

TITLE 16—Commercial Practices

CHAPTER II—CONSUMER PRODUCT SAFETY COMMISSION

SUBCHAPTER B—CONSUMER PRODUCT SAFETY ACT REGULATIONS

PART 1102—PUBLICLY AVAILABLE CONSUMER PRODUCT SAFETY INFORMATION DATABASE

rule

Subpart A—BACKGROUND AND DEFINITIONS

§1102.2
Purpose.
§1102.4
Scope.
§1102.6
Definitions.
rule

Subpart B—CONTENT REQUIREMENTS

§1102.10
Reports of harm.
§1102.12
Manufacturer comments.
§1102.14
Recall notices.
§1102.16
Additional information.
rule

Subpart C—PROCEDURAL REQUIREMENTS

§1102.20
Transmission of reports of harm to the identified manufacturer or private labeler.
§1102.24
Designation of confidential information.
§1102.26
Determination of materially inaccurate information.
§1102.28
Publication of reports of harm.
§1102.30
Publication of manufacturer comments.
rule

Subpart D—NOTICE AND DISCLOSURE REQUIREMENTS

§1102.42
Disclaimers.
§1102.44
Applicability of sections 6(a) and (b) of the CPSA.


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