Professional Documents
Culture Documents
0034/MSI/I- 2018
Type of Audit :
INITIAL
Head Office :
Jl. Letjend. Suprapto No. 55C, Ungaran
Kabupaten Semarang
CONFIDENTIAL
Phone : +62 24 7651 0101
Email : marketing@multisertifikasi.co.id
AUDIT REPORT
Ownership of this report and the information
contained within re main the property of
MSI Certification Body
Scope :
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Company Information
Company Name PT. MARGO TRESNO KARYA
Auditor Information
Lead Auditor Sindung Harsono
Auditor(s) - Expert -
Scope of Certification
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Recomendation of the audit team
The auditors confirm that they have not performed any management system consultancy to the audited
organization during the previous 2 years and that they will not perform any consultancy during the period of
certification and 2 years after. The auditors also confirm that there was no conflict of interest present during
the certification process.
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permit?
PERMEN No. 14/M-DAG/PER/2/2016 &
Licensing for Corporate Legal, PERMEN No. 77/M-DAG/PER/12/2013 Y
Business License, Permit Place of Y Licensing for Corporate Legal,
Business Business License and Business
Rules and regulations of Labor and Y
Y UU N0. 13, 2003, About Employment
Occupational Safety
Legislation related to marketing UU. No. 7, 2014 about the rules and Y
Y
licenses regulations of trade
UU. 18, 2012 abaut food safety and
Y
Product Quality Standards salable Y food industries
SNI 01-2802-1995 Flour Product
Permen No. 261/PMK.03/2016, abaut Y
legislation taxation Y tax
PERMEN No. 77/M- DAG/10/2014 Y
Legislation on Import Export Y Export Import Non Mineral
PERMEN P.43/Menhut-II/2014 &Permen
Y
Environmental Legislation Y LHK No. 68, 2016 use and control of
industrial waste
4. AUDIT PERFORMANCE
The practical implementation of the standard(s) was evaluated and compared with the management
system manual and supporting documents. The audit was conducted through discussions and
interviews with personnel at various locations and functions throughout the facility.
The audit covered relevant processes, areas of the organisation in order to obtain an overall picture of
the degree of management system implementation. Although performed to reasonable depth, not
every detail of the complete management system could be checked.
the management system has not adequately addressed nonconformity identified during previous
audit activities and the specific issue has been re-defined in the nonconformity section of this report.
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Note:
Changes which have influence on the validity of certification must be verified during the audit or, if necessary, in an additional
extension / verification audit. Examples of such changes have been explained in the closing meeting and the certification
contract.
Detailed audit findings, samples taken, audit trails followed etc. are included in the attached auditor
notes (Audit Trail)conduct and coverage of the audit is defined in theaudit plan and the attendance list
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8. AUDIT SUMMARY (ISO 9001:2015, ISO 14001:2015 & OHSAS 18001:2007)
The quality management system has been documented, implemented and maintained
accordance with ISO 9001:2015, ISO 14001:2015 & OHSAS 18001:2007 as well as statutory
and regulatory requirements. Top management having high commitment to meet with customer
requirement in order to increase the customer satisfaction.
Evidence :
Quality Manual was set : MM-YTN-01 rev 00
Date : 12 January 2016
By Mr. Adi Surya (Direktor)
No Negative Finding
Check Internal Audit Procedure : SOP-YTN/MR-02 rev 00, Internal audit already performed as
palnned on 7-9 January 2017 by internal auditors team who appointed by Top Management.
There are of audit covered all of the function and level within organizations. As the result of
internal audit already corrected properly. Corrective actions in order to prevent re occured of the
problems has been determined and will be verified in the next audit.
Evidence :
- Internal Audit Plan (Form-YTN/MR-02/01 rev 00)
- Auditor Team ((Form-YTN/MR-02/03 rev 00)
Mr. Hariyadi, Lead Auditor : Certificate of Internal Auditor Training No.
7838-PROXIS/2/2016
- Check List Audit (Form-YTN/MR-02/02 rev 00)
- Audit Result (Form-YTN/MR-02/05 rev 00), 3 minor 2 Obs, seen on the corrective action
was closed
Check Management Review Procedure : SOP-YTN/MR-03, rev 00 Top management already
reviewed the effectiveness of its quality management system implementation on 21 January
2017 with the inputs of review included the internal/external audit results, customer feedback,
performance of projects, achievement of quality objectives, corrective and preventive action
status, and follow up action of the prior management review. The results of review already
documented as required by procedure included corrective/preventive action plan, date for
implementation, needed resources and PIC.
Evidence ;
- Management Review Program (Form-YTN/MR-03/01 rev 00)
- MOM (Form-YTN/MR-03/03 rev 00)
- List of Participant of Management Review Program (Form-YTN/MR-03/08 rev 00)
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No Finding
HRD & GA
Check
1. Recruitment Procedure (SOP-YTN/HRD-01 rev 00)
2. Training Procedure (SOP-YTN/HRD-02 rev 00)
3. Job Disc and Evaluation Personnel
The job activities cover recruitments, staffing (job placement), regular training, on-the-job-
training, etc. The regular report prepared is to monitor personnel activities (i.e. attendance
record, performance achieved). The staff appraisal is conducted by annual basis. This is also
responsible for the up-grading competencies of internal staff, while the end-result (promotion,
demotion, and training) is subject to be decided by Manager. This unit is also responsible the
maintenance of working environment, such as computer, building renovation, security, Etc.
Evidence :
- Roles of company (DOK-YTN/ITR-3015)
- Employee Evaluation (Form -YTN/HRD-01/03 rev 00)
- Training Program and Realization (SOP-YTN/HRD-01/03 rev 00), 100% implemented
No finding
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No finding
Observation : Opportunities for improvement opportunities to make a planning documentation
and the achievement of sales to the local market (East Java) focus market on PLN (JAWA-BALI)
Production/Project
The production is responsible for the overall performance and control of product realization
according to customer requirements/specification (such as project quality Plan and compliance to
contract agreement). There are several stages that shall be completed by Manager prior to
execute of construction project, such as reviewing and studying carefully all customer
requirements/specifications as stipulated within document contract, preparing the availability of
materials, equipment, vehicles and human resources, all necessary legal/licence documents
relating to product requirements, etc.
No finding
Purchasing
The production is responsible for the overall performance and control of Purchashing realization
according to Plan & Departement/Unit requirements/specification (such as Production/project
quality Plan and compliance to contract agreement). There are several stages that shall be
completed by Manager prior to execute of production process and activities support, such as
purchas order form, spesification of goods, supplier, approval by finance manager or director,
reviewing and studying carefully all customer requirements/specifications as stipulated within
document contract, preparing the availability of materials, equipment, vehicles and human
resources, all necessary legal/licence documents relating to product requirements, etc.
No finding
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Maintenance
In general maintenance program implementation goes well, in accordance with planning in
charge of management, Risk Register has been set and in the value of the degree of risk, as well
as the visible implementation of risk reduction action is determined.
Visible part measurement quality objectives have been set and looks evaluations over the past
three months priceless nice
The main engine maintenance, support and calibrated machine that has been done properly in
accordance with a program that is in charge
No finding
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Audit Summary Matrix (QMS ISO 9001:2015)
Maintenance
Purchasing
Distribution
Production
Marketing
Activities
Logistic/
QC/QA
HRD
Total
ISO 9001:2015 Requirement
Auditor:
4 Context of organization
4.1 Understanding the organization and its context
Understanding the needs and expectations of
4.2
interested parties
Determining the scope of quality management
4.3
system
4.4 Quality management system and its processes
5.1 Leadership and commitment
5.1.1 General
5.1.2 Customer Focus
5.2 Policy
5.2.1 Developing the quality policy
5.2.2 Communicating the quality policy
5.3 Organizational roles, responsibilities and authorities
6 Planning
6.1 Actions to addressed risks and opportunities
6.2 Quality objectives and planning to achieve them
6.3 Planning of changes
7 Support
7.1 Resources
7.1.1 General
7.1.2 People
7.1.3 Infrastructure
7.1.4 Environment for operation of processes
7.1.5 Monitoring and measuring resources
7.1.5.1 General
7.1.5.2 Measurement traceability
7.1.6 Organizational knowledge
7.2 Competence
7.3 Awareness
7.4 Communication
7.5 Documented information
7.5.1 General
7.5.2 Creating and updating
7.5.3 Control of documented information
8 Operation
8.1 Operational planning and control
8.2
8.2.1 Requirements for products and services
Determining the requirements related to products
8.2.2 and services
Review of requirements related to products and
8.2.3 services
8.2.4 Changes to requirements for products and services
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8.3 Design and development of products and services
8.3.1 General
8.3.2 Design and development planning
8.3.3 Design and development inputs
8.3.4 Design and development controls
8.3.5 Design and development outputs
8.3.6 Design and development changes
Control of externally provided process, products and
8.4 services
8.4.1 General
8.4.2 Type and extent of control
8.4.3 Information for external providers
8.5 Production and service provision
8.5.1 Control of production and service provision
8.5.2 Identification and traceability
Property belonging to customers or external
8.5.3 providers
8.5.4 Preservation
8.5.5 Post-delivery activities
8.5.6 Control of changes
8.6 Release of products and services
8.7 Control of nonconforming outputs
9 Performance evaluation
9.1 Monitoring, measurement, analysis and evaluation
9.1.1
9.1.2 General satisfaction
Customer
9.1.3 Analysis and evaluation
9.2 Internal audit
9.3 Management review
9.3.1 General
9.3.2 Management review inputs
9.3.3 Management review outputs
10 Improvement
10.1 General
10.2 Nonconformity and corrective action
10.3 Continual improvement
ELEMENT ADDRESSED, NO CORRECTIVE
ACTION RAISED
Major Minor Observation
0 0 2
ELEMENT ADDRESSED, NUMBER OF
NUMBER CORRECTIVE ACTIONS RAISED
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9.AUDIT OUTCOME
The significant audit results are grouped in two (2) categories:
Non-conformity (NC), mandatory to be verified before issue or continuance of certification can be
recommended;
Major Nonconformity: The absence or total breakdown of a system to meet a requirement. (e.g.a failure
to achieve legal or statutory requirements, etc.). Solution: Corrective actions have to be done within 90
days and re- audit (on-site or off-site).
Minor Nonconformity:Any failure of the audited system to satisfy a written requirement that is not
considered to be a major nonconformity.
Solution: root cause analysis and definition of corrective actions within 90 days and verification of
documents (off-site).
Observation : Any potential condition that may become NC on next audit and the auditor wants to verifiy
it in the next audit and does not require immediate action (one work instruction not updated, qualification
matrix incomplete,etc.). Solution: Auditor has to get the acceptance signature from the customer and
verifiy in the next audit.
AUDIT FINDING
Company has well implemented the integrated management system QMS through conducting
01 internal audit, customer satisfaction and management review.
NO OBSERVATION AREAS
NON-CONFORMITY SITUATION
MAJOR/
NC NO. CLAUSE STD/SCHEME DESCRIPTION
MİNOR
None
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