SUBPART C—Procedural Requirements (§1102.20 to §1102.30)
- 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.