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HHS - 21 CFR PART 1003

NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY

active, Most Current
Organization: HHS
Publication Date: 1 April 2021
Status: active
Page Count: 5

Document History

21 CFR PART 1003
April 1, 2023
NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
A description is not available for this item.
21 CFR PART 1003
April 1, 2022
NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
A description is not available for this item.
21 CFR PART 1003
April 1, 2021
NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
A description is not available for this item.
21 CFR PART 1003
April 1, 2020
NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
A description is not available for this item.
21 CFR PART 1003
April 1, 2019
NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
A description is not available for this item.
21 CFR PART 1003
April 1, 2018
NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
Applicability. The provisions of this part are applicable to electronic products which were manufactured after October 18, 1968.
21 CFR PART 1003
April 1, 2017
NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
Applicability. The provisions of this part are applicable to electronic products which were manufactured after October 18, 1968.
21 CFR PART 1003
April 1, 2016
NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
Applicability. The provisions of this part are applicable to electronic products which were manufactured after October 18, 1968.
21 CFR PART 1003
April 1, 2015
NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
Applicability. The provisions of this part are applicable to electronic products which were manufactured after October 18, 1968.
21 CFR PART 1003
April 1, 2014
NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
Applicability. The provisions of this part are applicable to electronic products which were manufactured after October 18, 1968.
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References

This document is referenced by:
ASTM F3095 - Standard Practice for Laser Technologies for Direct Measurement of Cross Sectional Shape of Pipeline and Conduit by Rotating Laser Diodes and CCTV Camera System
Published by ASTM on December 1, 2017
This practice covers the procedure for the post installation verification and acceptance of buried pipe deformation using a visible rotating laser light diode(s), a pipeline and conduit inspection...
This document is referenced by:
C22.2 NO. 60601-1-2:16 - Medical electrical equipment — Part 1-2: General requirements for basic safety and essential performance — Collateral Standard: Electromagnetic disturbances — Requirements and tests
Published by CSA on January 1, 2016
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
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