21 CFR § 600.20 - Inspectors.

---
identifier: "/us/cfr/t21/s600.20"
source: "ecfr"
legal_status: "authoritative_unofficial"
title: "21 CFR § 600.20 - Inspectors."
title_number: 21
title_name: "Food and Drugs"
section_number: "600.20"
section_name: "Inspectors."
chapter_name: "FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES"
subchapter_number: "F"
subchapter_name: "BIOLOGICS"
part_number: "600"
part_name: "BIOLOGICAL PRODUCTS: GENERAL"
positive_law: false
currency: "2026-04-05"
last_updated: "2026-04-05"
format_version: "1.1.0"
generator: "[email protected]"
authority: "21 U.S.C. 321, 351, 352, 353, 355, 356c, 356e, 360, 360i, 371, 374, 379k-l; 42 U.S.C. 216, 262, 263, 263a, 264."
cfr_part: "600"
---


# 600.20 Inspectors.

Inspections shall be made by an officer of the Food and Drug Administration having special knowledge of the methods used in the manufacture and control of products and designated for such purposes by the Commissioner of Food and Drugs, or by any officer, agent, or employee of the Department of Health and Human Services specifically designated for such purpose by the Secretary.

[38 FR 32048, Nov. 20, 1973]