Food safety : FDA can better oversee food imports by assessing and leveraging other countries' oversight resources : report to congressional committees.

Format:

Book

Government document

Author/Creator:

United States. Government Accountability Office

Language:

English

Subjects (All):

United States. Food and Drug Administration--Rules and practice.

United States.

United States Food and Drug Administration.

United States. Food and Drug Administration.

Food--Safety measures--Government policy--United States.

Food.

Imports--Inspection--Government policy--United States.

Imports.

Food contamination--United States--Prevention.

Food contamination.

Food Contamination--legislation & jurisprudence.

Food Safety--methods.

Food contamination--Prevention.

Medical Subjects:

United States Food and Drug Administration.

Food Contamination--legislation & jurisprudence.

Food Safety--methods.

United States.

Genre:

Rules

Physical Description:

1 online resource (ii, 48 pages) : color maps

Other Title:

FDA can better oversee food imports by assessing and leveraging other countries' oversight resources

Place of Publication:

[Washington, D.C.] : U.S. Govt. Accountability Office, [2012]

Summary:

U.S. reliance on imported food increased from 2000 through 2011. For some products, imports make up a considerable share of the total amount consumed in the United States. FDA--responsible for ensuring the safety of most imported foods--received new authority under FSMA to enhance its oversight of food imports, including express authority to establish a system for accrediting third parties, which may include foreign governments and private auditing firms, to certify foreign food facilities' compliance with U.S. food safety requirements. FDA has also begun to assess selected foreign food safety systems to determine if these systems provide the same level of public health protection, among other things. GAO was asked to (1) identify major actions FDA is to take to implement a system for accrediting third parties and challenges, if any, it and others report with these actions and (2) examine FDA's approach for using comparability assessments to leverage other countries' oversight capacity and enforcement authority. GAO reviewed FDA documents and interviewed officials from FDA and other agencies, and stakeholders, such as consumer groups and industry representatives.

Notes:

Title from title caption (viewed on Dec. 31, 2012).

"September 2012."

Includes bibliographical references.

"GAO-12-933."

OCLC:

823385191