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Regulations (Standards - 29 CFR) - Table of Contents
• Part Number: 1987
• Part Title: PROCEDURES FOR HANDLING RETALIATION COMPLAINTS UNDER SECTION 402 OF THE FDA FOOD SAFETY MODERNIZATION ACT
• Subpart: B
• Subpart Title: Litigation
• Standard Number: 1987.108
• Title: Role of Federal agencies.
• GPO Source: e-CFR


1987.108(a)(1)

The complainant and the respondent will be parties in every proceeding and must be served with copies of all documents in the case. At the Assistant Secretary's discretion, the Assistant Secretary may participate as a party or as amicus curiae at any time at any stage of the proceeding. This right to participate includes, but is not limited to, the right to petition for review of a decision of an ALJ, including a decision approving or rejecting a settlement agreement between the complainant and the respondent.

1987.108(a)(2)

Copies of documents must be sent to OSHA and to the Associate Solicitor, Division of Fair Labor Standards, U.S. Department of Labor, only upon request of OSHA, or where the Assistant Secretary is participating in the proceeding, or where service on OSHA and the Associate Solicitor is otherwise required by the rules in this part.

1987.108(b)

The FDA, if interested in a proceeding, may participate as amicus curiae at any time in the proceeding, at the FDA's discretion. At the request of the FDA, copies of all documents in a case must be sent to the FDA, whether or not the FDA is participating in the proceeding.
[79 FR 8630, Feb. 13, 2014]

Next Standard (1987.109)

Regulations (Standards - 29 CFR) - Table of Contents

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