21 CFR 1230.32

§ 1230.32 Analyzing of samples.

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

Cite this

Citation: 21 CFR 1230.32, § 1230.32 Analyzing of samples, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/91645
Permanent ID: ys:prov:91645@1
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Full text

Samples collected by an authorized agent shall be analyzed at the laboratory designated by the Food and Drug Administration. Only such samples as are collected in accordance with §§ 1230.30, 1230.31 may be analyzed by or under the direction and supervision of the Food and Drug Administration. Upon request one subdivision of the sample, if available, shall be delivered to the party or parties interested.

Legislative history

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