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21 CFR 1.1108

§ 1.1108 When and how will FDA issue a directed food laboratory order?

United States · 21 CFR — Food and Drugs · Status: effective

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21 CFR 1.1108, § 1.1108 When and how will FDA issue a directed food laboratory order?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/82906
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(a) FDA may require the owner or consignee to conduct food testing, or to have food testing conducted on their behalf, under this subpart to address an identified or suspected food safety problem, as FDA deems appropriate. (b) The directed food laboratory order will specify the food product or environment to be tested; whether the food testing may be conducted using a LAAF-accredited laboratory that is owned, operated, or controlled by the owner or consignee; the timeframe in which the food testing must be conducted; and the manner of the food testing, such as the methods that must be used. (c) The directed food laboratory order will contain all the elements required by § 16.22(a) of this chapter and will thereby constitute the notice of an opportunity for hearing under part 16 of this chapter. An affected owner or consignee may request a regulatory hearing on a directed food laboratory order pursuant to § 1.1174.

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.