5,000 m²
factory area
Aluminum Bottle Manufacturing Factory in Vietnam
VAB operates an aluminum bottle manufacturing factory in Vietnam, supporting OEM projects that require clear production capability, controlled processes, and supplier evaluation documentation for B2B buyers.
- 5,000 m² factory
- 01 automated production line
- 3,000,000 bottles/month
01
automatic production line
3,000,000
bottles/month
FSSC 22000
ISO 9001 · FDA Registration
Overview
A production base for buyer validation
VAB is the aluminum bottle brand of GREEN PACKING MANUFACTURING TRADING IMPORT EXPORT CO., LTD, operating a factory in Vietnam for B2B and OEM aluminum bottle projects.
This page helps Procurement, QA/QC, Supply Chain, and Product Development teams quickly evaluate VAB’s production foundation before submitting an RFQ or requesting supplier documentation.
VAB focuses on aluminum bottle manufacturing for businesses that require customization, printing, sampling, and production based on confirmed specifications. The factory is not only where bottles are produced, but also the operating base for sample control, schedule coordination, quality checks, and project-related documentation.
- Manufacturing location: Vietnam.
- Legal entity: GREEN PACKING MANUFACTURING TRADING IMPORT EXPORT CO., LTD.
- External brand: VAB - VietNam Aluminum Bottle.
- Business model: B2B / OEM manufacturing.
- Core products: aluminum bottles and customized aluminum packaging solutions.
- Suitable buyers: food, beverage, cosmetics, personal care, pharmaceutical, healthcare, and products requiring packaging review based on technical requirements.
Infrastructure
Confirmed production infrastructure
VAB operates a 5,000 m² factory with 01 automatic production line and a confirmed production capacity of 3,000,000 bottles per month.
For B2B buyers, factory capability should be supported by verifiable information: factory area, production line, capacity, manufacturing scope, and order coordination capability.
Actual capacity for each project must be confirmed based on bottle specifications, capacity, accessories, customization level, printing requirements, approved samples, production schedule, and inspection standards. In other words, capacity is the foundation; real orders still need real specifications. Unfortunately, “urgent” is not a production specification.
- Factory area: 5,000 m².
- Production line: 01 automatic production line.
- Capacity: 3,000,000 bottles/month.
- Printing: offset printing up to 8 colors.
- Project model: OEM / private label / custom packaging.
- Confirmation factors: specifications, quantity, accessories, printing, samples, and production schedule.
Process
Manufacturing flow confirmed by project
VAB works with customers through defined steps: requirement intake, specification review, sampling, specification approval, production, inspection, and delivery.
An OEM aluminum bottle project should not start with pricing before product information, capacity, design, accessories, and inspection requirements are clear. Cost, MOQ, and lead time depend on these factors.
VAB’s working process is designed to help buyers confirm key points before mass production, especially for projects involving printing, accessories, coating, custom samples, or quality documentation.
- 1. Requirement intake: filled product, capacity, quantity, target market, and timeline.
- 2. Specification review: bottle, neck finish, cap, pump, spray, or related accessories.
- 3. Customization review: color, design, offset printing, surface finish, and finishing requirements.
- 4. Sampling: performed based on project scope and suitable production conditions.
- 5. Sample approval: confirmation of sample, specifications, inspection standards, and packaging requirements.
- 6. Production: implementation based on the agreed production plan.
- 7. Inspection: based on approved samples, technical specifications, and confirmed quality requirements.
- 8. Delivery: coordination of packaging, documentation, and schedule based on each order.
Control
Quality control points inside the factory
VAB approaches quality control based on specifications, approved samples, and customer-agreed requirements, not generic claims such as “leading quality.” Stunningly, buyers prefer evidence over adjectives.
Input
Material control
Requirements related to material, coating, or accessories need to be confirmed according to each product, project scope, and relevant technical documentation.
Process
In-process control
Production should follow approved specifications, reference samples, bottle requirements, and related inspection conditions to reduce the risk of variation.
Printing
Offset printing control
Printing designs need to be confirmed based on technical artwork, number of colors, print area, bottle surface, and approved samples before mass production.
Output
Final inspection before delivery
Finished products should be inspected based on agreed standards, including specifications, surface finish, printing, accessories, packaging, and documentation requirements when applicable.
Certifications
Certifications and scope must be understood correctly
VAB currently has FSSC 22000, ISO 9001, and FDA Registration. These certificates and registrations must be presented within their correct scope, not stretched into absolute quality claims.
The FSSC 22000 certificate issued by SGS covers a scope related to manufacturing aluminum packaging bottles intended for food industries. This is an important proof point for buyers evaluating the food safety management system within the certified scope.
FDA Registration is facility registration, not FDA Certification, FDA Approved Factory, or FDA Approved Products. The FDA Registration document also states that registration does not denote approval or authorization of the facility, its products, or product quality.
ISO 15378 is not currently available, so it must not be presented as an existing certification. If customers have pharmaceutical packaging, specialized packaging standards, or market compliance requirements, the applicable scope must be verified based on documentation and each order.
- FSSC 22000: used within the certified scope.
- ISO 9001: quality management system foundation.
- FDA Registration: facility registration, not product quality certification.
- ISO 15378: not currently available and must not be listed as an existing certification.
- Market compliance: must be verified based on specific customer requirements.
Documentation
Documentation support for factory evaluation
VAB supports buyers in factory evaluation with verifiable information: company profile, factory information, certifications, product specifications, and production documentation within the project scope.
Supplier evaluation usually does not stop at a quotation. Procurement and QA/QC teams need to know whether the supplier has a real factory, a clear production scope, relevant certifications, and the ability to provide necessary documentation during order implementation.
Depending on project requirements, VAB can coordinate the provision or verification of documents related to production capability, certifications, product specifications, approved samples, inspection standards, production records, and traceability within the applicable scope.
- Company documents: Green Packing legal entity, VAB brand, factory address, and contact information.
- Factory documents: factory area, production line, capacity, images, and manufacturing scope.
- Certification documents: FSSC 22000, ISO 9001, and FDA Registration within the permitted scope.
- Product documents: bottle specifications, accessories, printing, packaging, and approved samples.
- Production documents: production records within the project scope when applicable.
- Traceability support: information tracking within available production data and related documentation.
Buyer Check
What should buyers evaluate in a factory?
A suitable factory is not just a collection of nice images. Buyers should evaluate production capability, process control, quality systems, documentation, and RFQ response quality. Drone footage is lovely, but purchase orders do not run on drone footage.
Capacity
Production capability
Check factory area, production line, capacity, product scope, and the ability to support the actual specifications of the order.
Process
Project implementation process
Evaluate how the factory receives requirements, develops samples, approves specifications, produces, inspects, and manages changes before mass production.
Quality
Quality control
Review how the factory controls materials, production, printing, finished products, packaging, and related documentation based on agreed standards.
RFQ
RFQ response capability
A useful RFQ should include product information, capacity, quantity, accessories, design, target market, and timeline so the factory can confirm cost, MOQ, and lead time.
Frequently Asked Questions
The VAB factory is operated by GREEN PACKING MANUFACTURING TRADING IMPORT EXPORT CO., LTD in Vietnam. VAB is the external-facing brand for the company’s OEM aluminum bottle solutions.
The confirmed factory area is 5,000 m².
The confirmed production capacity is 3,000,000 bottles per month. The ability to support each order must be confirmed based on specifications, quantity, accessories, printing, customization level, and production schedule.
Yes. VAB has 01 automatic production line. The actual implementation scope must be confirmed based on product requirements and the production plan for each order.
Yes. VAB can support buyers with factory information, company documents, certifications, product specifications, related images, and production documents applicable to the project scope.
VAB currently has FSSC 22000, ISO 9001, and FDA Registration. The FSSC 22000 certificate issued by SGS covers a scope related to manufacturing aluminum packaging bottles intended for food industries.
No. FDA Registration is facility registration. It is not FDA Certification, FDA Approved Factory, or FDA Approved Products. The FDA Registration document also states that registration does not mean FDA approval or authorization of the facility, its products, or product quality.
No. The website must not present ISO 15378 as an existing certification. If customers have pharmaceutical or specialized packaging standard requirements, the applicable scope must be verified based on technical documentation and target market requirements.
Buyers should provide the filled product, desired capacity, quantity, cap or pump requirements, printing design, target market, documentation requirements, and expected timeline.
No. Suitability must be evaluated based on product characteristics, material, coating, accessories, usage conditions, inspection standards, and market requirements.
Request a Quote
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.