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The Code of Federal Regulations (CFR) annual edition is the codification of the general and permanent rules published in the Federal Register by the departments and agencies of the Federal Government produced by the Office of the Federal Register (OFR) and the Government Publishing Office.


Parallel Table of Authorities and Rules for the Code of Federal Regulations and the United States Code
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Electronic Code of Federal Regulations

Electronic Code of Federal Regulations

e-CFR data is current as of April 22, 2015

Title 21Chapter ISubchapter IPart 900


TITLE 21—Food and Drugs

CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

SUBCHAPTER I—MAMMOGRAPHY QUALITY STANDARDS ACT

PART 900—MAMMOGRAPHY

rule

Subpart A—ACCREDITATION

§900.1
Scope.
§900.2
Definitions.
§900.3
Application for approval as an accreditation body.
§900.4
Standards for accreditation bodies.
§900.5
Evaluation.
§900.6
Withdrawal of approval.
§900.7
Hearings.
§§900.8-900.9
[Reserved]
rule

Subpart B—QUALITY STANDARDS AND CERTIFICATION

§900.10
Applicability.
§900.11
Requirements for certification.
§900.12
Quality standards.
§900.13
Revocation of accreditation and revocation of accreditation body approval.
§900.14
Suspension or revocation of certificates.
§900.15
Appeals of adverse accreditation or reaccreditation decisions that preclude certification or recertification.
§900.16
Appeals of denials of certification.
§900.17
[Reserved]
§900.18
Alternative requirements for §900.12 quality standards.
rule

Subpart C—STATES AS CERTIFIERS

§900.20
Scope.
§900.21
Application for approval as a certification agency.
§900.22
Standards for certification agencies.
§900.23
Evaluation.
§900.24
Withdrawal of approval.
§900.25
Hearings and appeals.

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