Iso900 1 quality system certification is valid for three years. But the premise is that the enterprise must accept the supervision and audit of the certification body, that is, the annual review; The frequency of supervision and audit is generally1February, that is, once a year, so it is called annual review; Some enterprises may be special, and the certification body requires annual review once every 6 months or 10 months; ISO certification audit will be notified in advance, and some certifications are flight inspections, that is, unannounced inspections may arrive at the factory at any time.

Matters needing attention in the annual examination of iso900 1 system certification certificate

1, file part: file ledger, controlled file issuing and receiving records, invalid file recycling records, file change approval records, foreign file directory, file identification, etc.

2. Production part: production flow chart, production site operation instruction, various inspection records, personnel training records, special post training, assessment and work permit.

3. Procurement part: supplier information, including supplier classification, annual inspection records, various licenses and qualification certificates, procurement list, etc.

4. Human resources: recruitment requirements, recruitment plans, recruitment performance appraisal records, etc.

5. Equipment part: incoming inspection of equipment, daily inspection records of equipment, regular inspection, and operation personnel on duty.

6. Production planning and sales: production planning records, storage records, customer satisfaction survey records, etc.

7. Audit part: internal audit plan, internal audit checklist, internal audit meeting minutes, internal audit report, etc.

8. Management by objectives: the company's quality policies and objectives, the implementation of various departments, etc.

legal ground

Article 7 The product certification certificate shall include the following basic contents:

(1) The name and address of the client;

(2) Product name, model and specification, and description of product functions and characteristics when necessary;

(3) product trademark, manufacturer's name and address;

(4) The name and address of the product manufacturer;

(5) Standards and technical requirements on which the certification is based;

(6) authentication method;

(7) certificate number;

(eight) the issuing authority, issuing date and validity period;

(9) Other contents that need to be explained.