Cig 023 Form PDF Details

Navigating the complexities of factory inspections, the CIG 023 form stands as a cornerstone document for ensuring compliance and maintaining standards within manufacturing environments. Designed as a PERMANENT DOCUMENT by the revered Underwriters Laboratories Inc., this factory inspection report is instrumental only when deployed by ECS members and their authorized agents. With a clear caveat, the document underlines its authenticity and exclusivity, cautioning against unauthorized use. The content warns users about the limitations regarding endorsements, errors, or inaccuracies, stressing that UL abstains from assuming responsibility in these realms. Not merely a form, but a comprehensive guide, it encompasses a thorough inspection framework spanning across various sections inclusive of a detailed report form, inspector evaluations, and test data sheets, alongside precise identification criteria for selected samples. Furthermore, it underscores important procedural guidelines, urging inspectors to evaluate production processes even in their absence and stipulate detailed findings and rationale for any deviation from the norm. Indeed, the form exemplifies a meticulous approach towards maintaining quality and safety in manufacturing practices, ensuring that entities adhere to the expected standards, whilst clearly delineating the accountability lines. However, it's crucial to comprehend the structured methodology it advocates—right from verifying purchased components to maintaining robust incoming inspection records—all underscored by a steadfast commitment to accuracy and integrity in the inspection process.

QuestionAnswer
Form NameCig 023 Form
Form Length25 pages
Fillable?No
Fillable fields0
Avg. time to fill out6 min 15 sec
Other namescig023, ies, cig023 blank report, cig 023 factory inspection report

Form Preview Example

CIG 023

Factory Inspection

Report

PERMANENT DOCUMENT

CIG 023

Factory Inspection Report

WARNING:

THIS DOCUMENT IS ONLY VALID IF USED BY ECS MEMBERS

AND THEIR AUTHORISED AGENTS

UL does not endorse any vendors or products referenced herein.

UNDERWRITERS LABORATORIES INC. ASSUMES NO RESPONSIBILITY FOR ANY OMISSIONS OR ERRORS OR INACCURACIES WITH RESPECT TO THIS INFORMATION. UL MAKES NO REPRESENTATION OR WARRANTY OF ANY KIND WHATSOEVER, WHETHER EXPRESS OR IMPLIED, WITH RESPECT TO THE ACCURACY, CONDITION, QUALITY, DESCRIPTION, OR SUITABILITY OF THIS INFORMATION, INCLUDING ANY WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE AND EXPRESSLY DISCLAIMS THE SAME.

Copyright Underwriters Laboratories Inc. All rights reserved. May not be reproduced without permission. This document is controlled and has been released electronically. The version on the UL intranet is the up-to-date document. Hard copies are uncontrolled and may not be up-to-date. Users of hard copies should confirm the revision by comparing it with the electronically controlled version.

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CIG 023

Factory Inspection

Report

PD CIG 023 reports shall not contain any unauthorised modifications which change the

original meaning or the requirements.

Any additions created to any document in the series shall be shown in an Appendix.

This document contains:

two cover pages

a report form of 14 pages

Inspector’s Evaluation – Findings

Inspector’s Evaluation - Informative

TEST DATA SHEET- Product Verification Test

TEST DATA SHEET Routine Tests

IDENTIFICATION OF SELECTED SAMPLE

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CIG 023

Factory Inspection

Report

Reference number of the body carrying out the inspection:

FACTORY INSPECTION REPORT

Inspection carried out by (Name of Inspection Body):

Reference number of the Body carrying out the inspection:

For page control, please write this number in the header of each page (including the attachments)

GENERAL GUIDANCE

The questions of this factory inspection report are based on the requirements given in Permanent Document CIG 021.

Guidance for the inspector is given in Permanent Document CIG 024.

Both documents, PD CIG 021 and PD CIG 024 shall be taken into account during inspection.

Instructions to the Inspector are shown in italics

The report shall be completed even if there is no production at the time of the visit.

For all NOanswers details shall be provided on the INSPECTORS EVALUATION-Findings page

For all N/Aanswers rationale shall be provided as to why the item is not applicable

Details should be given on INSPECTOR’S EVALUATION-Informative page.

1.0 GENERAL INFORMATION

1.1Manufacturer's registered name and factory location

Manufacturer’s registered

name:

Street address of the factory and Number:

Postal code:

City:

County:

Country:

GPS-coordinates: (optional)

1.2Manufacturer's representative name and contact data

Manufacturer's representative name:

Position:

Position:

Telephone:

Fax:

E-Mail:

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CIG 023

Factory Inspection

Report

Reference number of the body carrying out the inspection:

1.3Record below the names and position held of the main people involved in the inspection

same as mentioned under 1.2

If not the same as mentioned under 1.2 please give details

Name:

Position:

Telephone:

Fax:

E-Mail:

1.4

Pre-Licence

Routine

ENEC

HAR

EMC

Others:

 

 

 

1.5Pre-Licence only: Is the information given in the Questionnaire CIG 022 Section B accurate and complete?

If 'no', amend the Questionnaire as appropriate and attach a copy to this report.

YES N/A

NO

1.6Inspection Details:

Certification

Inspection

File Reference

Body

X of Y

No.

requesting

 

 

inspection

 

 

 

 

 

Product

Category

Type of Product

1.7

Name of Inspector

Date of inspection:

(YYYY MM DD )

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CIG 023

Factory Inspection

Report

Reference number of the body carrying out the inspection:

2Verification of purchased components and materials which have a safety implication on the certified product (Incoming Inspection)

2.1 Are materials, components and sub-assemblies verified by the

YES

N/A

NO

manufacturer as complying with appropriate specification?

 

 

 

 

 

 

 

 

 

 

 

2.2 Does this verification also include the verification of the Certification

YES

N/A

NO

Marks?

 

 

 

 

 

 

 

 

 

 

 

Description of procedure (one or more boxes may be ticked)

 

 

 

Rely on suppliers’ out-going inspection / Suppliers’ quality plan

 

 

 

Audit conducted at the suppliers’ premises

 

 

 

Supplier control based on manufacturers’ check list

 

 

 

Conduct own incoming inspection

 

 

 

Identification check

 

 

 

Checked for correct type

 

 

 

Comparison to a reference

 

 

 

Rating

 

 

 

Certification mark

 

 

 

Certificate of conformity

 

 

 

Others

 

 

 

Details given on INSPECTOR’S EVALUATION-Informative page

 

 

 

Description of the procedure or ref. of documented procedure & revision or issue date:

Details are given on INSPECTOR’S EVALUATION-Informative page.

2.3

If the manufacturer relies on Certificates of Conformity, do they clearly

YES

N/A

NO

 

identify the product, quantity of items covered, the specification to which

 

 

 

 

the products conform, the production date and are they properly issued?

 

 

 

 

 

 

 

 

 

 

 

 

 

2.4

Is there a procedure covering the way to handle non-conforming

YES

N/A

NO

 

components and materials?

 

 

 

Description of the procedure or ref. of documented procedure & revision or issue date:

Details are given on INSPECTOR’S EVALUATION-Informative page.

2.5

Is the procedure and the way in which it is applied satisfactory?

YES

N/A

NO

 

(e.g.: components and materials clearly identified and/or segregated to

 

 

 

 

prevent unauthorised use?)

 

 

 

 

 

 

 

 

 

 

 

 

 

2.6

Are records of the incoming inspection maintained and satisfactory?

YES

N/A

NO

 

 

 

 

 

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