Records and Reports

United States · Last verified: 2026-09-08

Number

21 CFR 1002

Type

Regulation

Issuer

U.S. FDA

Status

in_force

Authority

FDA / CDRH

What this covers

电子产品的记录与报告：列名电子产品制造商须提交的产品报告、意外辐射事故报告，以及制造商、经销商和分销商应保存的记录和豁免情形。

Source: U.S. Food and Drug Administration (public domain)