VAB currently has FSSC 22000, ISO 9001, and FDA Registration, supporting B2B customers in evaluating quality management, food safety management, production records, and information traceability within the appropriate scope of each project.
VAB uses current certifications and registration within their correct scope, helping customers evaluate management systems before starting an OEM project.
FSSC 22000 supports the evaluation of VAB's food safety management system within the scope of manufacturing aluminum packaging bottles intended for the food industry.
ISO 9001 supports the evaluation of VAB's quality management system, operating processes, process control, and ability to meet customer requirements.
FDA Registration is facility registration. It is not product quality certification, not FDA Certified, and not FDA Approved Products.
VAB can support production records and information traceability within the appropriate scope of each project, each order, and verifiable production data.
For B2B customers, certifications help evaluate management systems, quality risk, and the ability to support long-term order implementation.
For OEM aluminum bottle projects, especially in food, beverage, cosmetics, personal care, and export products, customers often need to verify a supplier's management systems before placing an order.
VAB currently has FSSC 22000, ISO 9001, and FDA Registration. These certifications and registration support supplier evaluation within the appropriate scope, but they do not replace product specification confirmation, approved samples, inspection standards, order documentation, or specific market requirements.
FDA Registration must be understood correctly: it is facility registration, not FDA Certified, not FDA Approved Factory, and not FDA Approved Products.
For some international customers, especially those related to the U.S. market, FDA Registration may be part of supplier document review.
However, FDA Registration is not product quality certification. It should not be written or understood as FDA Certified, FDA Approved Factory, or FDA Approved Products. Facility registration also does not mean that FDA has approved the facility, its products, or product quality.
Beyond certifications, B2B customers often need to review production records, inspection standards, and information traceability by order.
Approved samples can be used as references for mass production, quality control, printing, accessories, and packaging.
VAB can support production records within the appropriate scope of each project, each order, and verifiable production data.
Inspection records may relate to appearance, printing, accessories, packaging, and inspection standards agreed before production.
Information traceability is supported within the scope of production data, shipment records, order documentation, and applicable project requirements.
To help VAB respond correctly to certification document requests, customers should provide the product, target market, document purpose, and type of documents required.
Each customer may need documents for different reasons. Some need certifications for supplier evaluation, some need records for internal QA/QC review, and others may need information for import, audit, or new product implementation.
VAB can coordinate document provision or verification within the appropriate project scope and verifiable data. Specific document requirements should be submitted early to avoid issues at the final stage of an order.
VAB currently has FSSC 22000, ISO 9001, and FDA Registration. These documents should be used within their correct certification or registration scope.
FSSC 22000 supports the evaluation of VAB's food safety management system, especially for packaging projects related to food and beverage products.
ISO 9001 focuses on quality management systems, operating processes, process control, and the ability to meet customer requirements.
No. FDA Registration is facility registration. It is not product quality certification, not FDA Certified, not FDA Approved Factory, and not FDA Approved Products.
VAB can support production records and information traceability within the appropriate scope of each project, each order, and verifiable production data. The documentation scope should be confirmed before production or before documents are sent to customers.
Customers can request certification documents. Document sharing depends on project scope, purpose of use, document sharing policy, and applicable verification requirements.
No. Certifications support management system evaluation, but they do not replace approved samples, product specifications, inspection standards, production records, or order-specific quality requirements.
Customers should provide product information, target market, document purpose, documents required, traceability requirements, and timing so VAB can respond within the correct scope.
Share your project information and requirements so the VAB team can review and provide an initial response based on your business needs.
For a more effective discussion, please provide information such as product type, capacity, expected volume, target market, technical requirements, and any supporting documents if available.
