For The Inspection Methods And Inspection Standards of The Massage Chair Third Party Inspection Service Made-in-china Product Inspection Service

For The Inspection Methods And Inspection Standards of The Massage Chair Third Party Inspection Service Made-in-china Product Inspection Service

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Model:
third party inspection service
Brand:
Massage chair inspection
Code:
product inspection service

Consumer Goods Inspection We help to ensure the quality, safety and sustainability of consumer products to satisfy regulatory requirements as well as the demands of the market. Third-party inspection of consumer products is a crucial step in a global quality assurance program to ensure the product meets quality and specification prior to shipment and market. YSI holds a team of trained full-time inspectors across all categories of consumer goods and located in all around China and Southeast Asia in support of client inspection needs. Control de calidad de carga de contenedores y servicio de inspección de Pre embarque de terceros, encuentre información detallada sobre Control de calidad de carga de contenedores y servicio de inspección de Pre embarque de terceros, servicio de inspección de terceros servicio de prueba profesional

Product Description

Standard for inspection of massage chairs

People who work tired for a day return home and collapse on the sofa refused to get up, more and more young people conservative spinal disease, cervical spondylosis trouble, so many families also began to have the existence of massage chair. How to inspect the massage chair? For the inspection methods and inspection standards of the massage chair, please see the following:

First, environmental inspection

The temperature is good at 5℃~40℃

The relative humidity should be less than or equal to 80

The prescribed voltage is 220 V±22V and the prescribed frequency is 50Hz±1Hz

Two, performance inspection

Apply 80% of the rated voltage to the massage chair, and it can operate normally.

Voltage fluctuation influence:

Under the condition that the working voltage is ±10% of the rated voltage, the massage chair does not appear abnormal sound and extra vibration, and it works normally.

Iii. Appearance inspection

In appearance, no obvious scars, cracks, stains, rust and other defects that reduce the performance were observed.

The parts shall be assembled according to the requirements of drawings and working instructions. There is no missing or missing assembly phenomenon, and the wrong installation direction shall not occur. All screws are installed according to the specified torque. Must be firmly screwed, not loose, shall not appear floating, stripping phenomenon. The words and ICONS on the nameplate should be bright and clear, without any words or wrong words.

Four, safety performance

① Leakage current detection at room temperature

At room temperature, the leakage current between any pole of the power supply and the basic protective and isolated metal parts and plastic housing is 3.5mA.

(2) Electrical strength detection at room temperature

At room temperature, the massage chair should be able to withstand 1250V and 50Hz between any pole of the power supply and the metal parts of basic protection and isolation. After 1min of experimental voltage, there is no flashover and breakdown phenomenon.

③ Leakage current at operating temperature

When the massage chair works to a stable state, the leakage current between any pole of the power supply and the metal parts and plastic shell of the basic protection and isolation is 3.5mA.

(4) Electrical strength at working temperature

After working to a stable state, any pole of the power supply and the metal parts of basic protection and isolation should be able to withstand the experimental voltage of 1000V and 50Hz for 1min without flashover and breakdown phenomenon.

5. Factory inspection

Inspection of type

Type test must be carried out under any of the following circumstances

① A new trial-produced product

② When the design, process, material changes affect the product performance

③ When a product is produced again after a year's suspension

④ When the product is transferred to the factory

(5) Batch products are inspected regularly once a year

⑥ Similar products evaluation.

The type test of massage chair shall not be less than 1 sets each time.

Criterion of judgment

① The occurrence of a non-accidental failure is judged as unqualified.

(2) If the fault category cannot be determined, the number of faults will be included in the total number of faults, and another prototype should be extracted to carry out the whole test of the project again. If the same fault occurs, the test will be judged as unqualified. If other occasional faults occur, they will be included in the total number of faults in the test.

③ Repair is allowed for accidental failures. All tests of the performance item should be reconducted after repair.

Vi. Mark and specification inspection

mark

Nameplates must be fixed on the designated position of each massage chair. Each nameplate should indicate the product name, model, rated voltage, rated input power or rated current, rated frequency, factory number, manufacturer name or label. In addition, there must be corresponding instructions and warning signs in the relevant parts of the massage chair.

It mainly includes:

Pre-production Inspection (PPI)

A visual check on the quality of components, materials, and accessories at the beginning of production against clients' specifications and/or reference sample. The PPI thus permits timely corrections and improvements before the mass cargo will be manufactured, any non-conformity is immediately reported so as to avoid delay in shipment. In general, we will check the following aspects for PPI:
Evaluate the production status during the manufacturing process
Randomly inspect the finished samples on-site and compare them with your product spec
According to the evaluated status of finished and semi- finished samples, rearrange the QC layout in the factory.
Evaluate the packing details and packing material
Check the accuracy of production equipments and disposal methods for defective goods

100% inspection (Full Inspection)

When the merchandise is 100% completed, we will check the quality of goods unit by unit, which covers product description, style &color, workmanship, quality, function, label, package, size measurement if available etc, to make sure 100% of the goods meet your specified quality requirement. Note: for those products of high value or complicated internal structure, we suggest to take full inspection.

Container Loading Supervision (CLS)

Before loading, our inspector will check products' information, qty, package, during the course of loading, our inspectors will keep closely look at the loading process, ensure that the export cartons are well arranged in the container with no risks of deformation, collapse, help manufacturer finish loading under correct and clear working clauses and working process. In general:

Record the weather/arrival time of container/No./truck No Check the inner/outer condition to see if there is any
damage/wet/hole/peculiar smell Check the qty of goods loaded and record the condition of outer packaging(master cartons/pallets).Randomly draw and open some cartons to verify that the goods meet with clients' specification Supervise the whole loading process.Seal the container with the custom's seal and unique quality inspection's seal Record the seal No. and departure time of container.

Random Inspection

(Pre-production Random Inspection, During Production Random Inspection, Pre-shipment Random Inspection) As per customer's quality requirement, we will sample the products according to international or other standards to inspect the packing, appearance, color, size, function, safety, etc.
Purpose of Pre-production Random Inspection: To help know the production status & raw material quality and avoid any mistake on quality standard, order quantity and make sure that the order is arranged;
Purpose of During Production Random Inspection: To help know the production status & product quality during production and avoid any mass quality problem & abnormal production situation;
Purpose of Pre-shipment Random Inspection: To know the finished products quality & quantity and avoid any mass quality problem & shortage shipment.

What do our QC inspectors (quality inspector) do for the inspections ?

1. Confirm the quantity of the products.

2. Confirm the packing detail information of the products.

3. Check the information or marks reqiured by clients, such as the information on the carton, information on gift box, information
on products, warning text and all the others.

4. Check the overall appearance of the product.

5. Check the conmponents of the products.

6. Perform the general tests.
(1) General function test.
(2) Dimension of packing or products.
(3) Gross weight or net weight.
(4) Carton drop test.
(5) Barcode number test.

7. List all the defects of products found during the inspection.

8. Any other work that clients want us to do during the inspection.

1.Why do I need shipment inspections or factory audits?
In case of any Poor quality, incorrect shipments, unreal information from suppliers. Inspection is the most efficient way to protect buyer’s right.

2.How to start the inspection?

(1)Book an Service 2-3 days in advance.

(2)Pay us the cost before inspection.

(3)Start inspection/audit work on the booked date.

(4)Send you reports within 24 hours after inspection.

(5)Continuing Services after inspection

3.What information does the inspection report include?
Our written reports are very detailed, including accurate description of all defects and inconsistencies, statistic analysis based
on the highly recognized AQL standard and plentiful spot pictures for illustration.A written report + Original pictures will provided within 12hours after inspection.

4.How can I get a rapid quotation?

Getting a rapid quotation should have a complete condition,such as gross weight size,quantity and where is the factory and where will it ship to."

What testing is required for my product?

Regulatory laws and guidelines are an increasing challenge to importers through the world. How these affect you will vary widely based on your product type, component materials, where the product is being shipped, and the end-users in your market. Since the risk is so high, it is imperative you stay up to date on all relevant regulatory laws affecting your products. YONGSHUN staff can work with you to determine your exact requirements and propose a custom solution to best meet your needs. We also provide monthly updates on regulatory matters to keep our customers informed. Feel free to use the contact form to get on our newsletter list.
How can I get updates on regulatory issues?

YONGSHUN takes great pride in our technical brain trust. They are constantly updating our internal knowledge base so we are prepared to proactively inform our customers on issues affecting their products. In addition, each month we send out our Product Safety and Compliance Update. This is a comprehensive view into the latest industry and regulatory changes and recall review that helps you make critical decisions. We invite you to join our list of recipients. Use the Contact Us form to get on the list to receive it.
Is package testing necessary for all products?

Package testing is mandated by regulations for some products such as; food, pharmaceuticals, medical devices, dangerous goods, etc. This may cover both the design qualification, periodic retesting, and control of the packaging processes. For unregulated products, testing may be required by a contract or governing specification. However, for most consumer goods, package testing is often a business decision involving risk management for factors such as:

• cost of packaging
• cost of package testing
• value of package contents
• value of good will in your market
• product liability exposure
• other potential costs of inadequate packaging

YONGSHUN staff would be happy to assess your specific product and packaging requirements to help you determine whether package testing can improve your quality deliverables.
How can California Prop 65 affect my business?

Prop 65 is the 1986 voter-approved Safe Drinking Water & Toxic Enforcement Act that includes a list of Chemicals known to the State of California to cause cancer and/or reproductive toxicity. If a product contains a listed chemical, then the product must contain a “clear and reasonable” warning label informing consumers of the presence of the chemical and stating the chemical is known to cause cancer, birth defects, or other reproductive harm.

Although companies with fewer than 10 employees are exempt, if they sell a violative product to a retailer with more than 10 employees, the retailer could receive a notice of violation. In these circumstances, retailers usually rely on clauses within their contacts with importers that require the importer take responsibility for the violation.

A plaintiff may seek injunctive relief requiring a company caught selling a violative product to suspend sales, conduct a recall, or reformulate the product. Plaintiffs can also obtain penalties of up to $2,500 per violation per day. A more general California statute allows most successful plaintiffs to recover their attorneys’ fees as well.

Many are now choosing to rely on 3rd party testing companies to verify that hazardous substances are not being used in their products.
How can my products meet regulatory requirements for hazardous chemicals?

The simplest way is to engage a 3rd party testing company, such as YONGSHUN. Some manufacturers self-test and/or rely on local testing labs for certifying their products. However, there is no guarantee these labs, or their equipment, are reliable. Nor is there any guarantee the results are accurate. In either case, the importer may be held responsible for the product. In view of the risk, most companies opt to use a 3rd party testing lab. YONGSHUN’ 80,00 sf laboratory is centrally located in Hangzhou China, and does a broad range of consumer goods for all regulatory testing requirements.
What should I know about my supplier?

Doing business in Asia can be a tricky and expensive effort if sufficient due diligence is not done for a supplier. How much is required may depend on your buyer’s requirements, your personal commitment to social compliance, and other business needs. YONGSHUN provides supplier evaluations and factory audit services from simple evaluation to complex technical and social compliance audits. YONGSHUN staff can work with you to determine your exact requirements and propose a custom solution to best meet your needs.
Why is a factory audit or supplier evaluation important?

Do you REALLY know who you are buying from? Do you REALLY know what their production capabilities are and whether they can produce what you expect? These are important questions when assessing a potential vendor. Asia is ripe with middlemen, sub-contracting, materials and component swapping, fraudulent certifications and licensing, and sub-standard facilities, materials, and equipment. The only way to be sure who your supplier is and what his capabilities are, is to do an onsite evaluation or audit. YONGSHUN has experienced professional staff that are ready to conduct your factory audit supplier evaluation. Contact us today for details on the broad range of audit and evaluation types we can provide for you.
How do you monitor your inspectors work?

YONGSHUN has a dynamic inspector and auditor training and audit program. This includes periodic retraining and testing, unannounced visits to factories where quality control inspections, or factory audits, are being conducted, random interviews with suppliers, and random audits of inspector reports as well as periodic efficiency audits. Our inspectors program has resulted in developing staff of inspectors that are among the best in the industry, and our competitors frequently try to recruit them away.
What kind of inspections do I need?

The type of quality control inspection you need largely depends on the quality goals you are trying to achieve, the relative importance of quality as it relates to your market, and whether there are any current production issues that need to be resolved.

We invite you to explore all the inspection types we provide by clicking here.

Or, you can contact us, and our staff can work with you to determine your exact requirements, and propose a custom solution to best meet your needs.
What does AQL mean?

AQL is the acronym for Acceptable Quality Limit (or Level). This represents a statistical measurement of the maximum number and range of defects that is considered acceptable during a random sampling inspection of your goods. If the AQL is not achieved for a particular sampling of goods, you may accept shipment of the goods ‘as is’, demand a rework of the goods, renegotiate with you supplier, refuse the shipment, or choose another recourse based on your supplier agreement.

Defects found during a standard random inspection are sometimes classified into three levels: critical, major and minor. Critical defects are those that render the product unsafe or hazardous for the end user or that contravene mandatory regulations. Major defects can result in the product’s failure, reducing its marketability, usability or salability. Lastly, minor defects do not affect the product’s marketability or usability, but represent workmanship defects that make the product fall short of defined quality standards. Different companies maintain different interpretations of each defect type. Our staff can work with you to determine the AQL standard that meets your requirements according to the level of risk you are willing to assume. This becomes the primary reference during a pre-shipment inspection.

It is important to note; the AQL inspection is only a report on the findings at the time of the inspection. YONGSHUN, like all 3rd party QC companies, does not have the authority to make a decision as to whether your goods can be shipped. That is a decision only you can make in consultation with your supplier after reviewing the inspection report.