IEEE 567-1980 PDF

IEEE 567-1980 PDF

Name:
IEEE 567-1980 PDF

Published Date:
10/17/1980

Status:
[ Withdrawn ]

Description:

IEEE Trial-Use Standard Criteria for the Design of the Control Room Complex for a Nuclear Power Generating Station

Publisher:
IEEE

Document status:
Active

Format:
Electronic (PDF)

Delivery time:
10 minutes

Delivery time (for Russian version):
200 business days

SKU:

Choose Document Language:
$15.9
Need Help?
New IEEE Standard - Inactive-Withdrawn. This standard addresses the central control room of nuclear power generating station and the overall complex in which this room is housed. It is not intended to cover special or normally unattended control rooms, such as those provided for radioactive waste handling or for emergency shutdown operations.
File Size : 1 file , 890 KB
ISBN(s) : 9780738142302
Note : This product is unavailable in Russia, Belarus
Number of Pages : 16
Product Code(s) : STDWD95464
Published : 10/17/1980

History


Related products

IEEE 765-2022
Published Date: 04/29/2022
IEEE Standard for Preferred Power Supply (PPS) for Nuclear Power Generating Stations (NPGS)
$17.7
IEEE 317-2013
Published Date: 07/17/2013
IEEE Standard for Electric Penetration Assemblies in Containment Structures for Nuclear Power Generating Stations
$33
IEEE 628-2020
Published Date: 04/15/2020
IEEE Standard Criteria for the Design, Installation, and Qualification of Raceway Systems for Class 1E Circuits for Nuclear Power Generating Stations
$20.4

Best-Selling Products

MEDDEV 13/93
Published Date:
Guidelines Relating to the Application of: The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices
MEDDEV 2.1/3
Published Date: 03/01/1998
Guidelines Relating to the Demarcation Between 90/385/EEC on Active Implatable Medical Devices, 93/42/EEC on Medical Devices,65/65/EEC Relating to Medicinal Products & Related Directives
MEDDEV 3/94
Published Date: 04/01/1994
Guidelines Relating to the Application of : The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices