In-house perfume manufacturing
Our perfume factory & protected documentation
Our factory brings fragrance projects into production.
ARQUENOR manufactures Dupe Fragrances, develops Custom Fragrance projects from a formula brief or customer-provided sample, and delivers Private Label, OEM and ODM Packaging Solutions in our own production facility.
Factory-directFragrance evaluation, filling, assembly, packaging and document review
Current typical starting quantity
Production and utility systems shown below
Current full documents for qualified buyers
Company & facility identity
The company behind the ARQUENOR project.
ARQUENOR is the project and customer-facing name used on this website. The legal operating entity is Xiamen Fairmont Fragrance House Co., Ltd., with its perfume factory located in Xiamen, Fujian, China.
- Project name
- ARQUENOR
- Legal entity
- Xiamen Fairmont Fragrance House Co., Ltd.
- Factory location
- Xiamen, Fujian, China
Factory-direct manufacturing
Developed, filled and packed in our own perfume factory.
The facility images on this page show our own perfume manufacturing environment, including fragrance evaluation, controlled workshop, filling, component handling, assembly, packaging and supporting utility areas.
Our commercial and production teams coordinate Dupe Fragrances, Custom Fragrance development and Private Label, OEM or ODM Packaging Solutions through manufacturing and inspection. Exact scope, component availability, capacity and schedule are confirmed during quotation.
Inside our factory
From controlled workshop to final packing.
These images show how an approved private-label specification moves through our filling, assembly and packaging environment.
Installed equipment
Close-range equipment views from our facility.
These factory photographs add equipment-level context to the wider workshop views. The machinery and setup assigned to an order depend on its bottle, closure, formula and packaging specification.
01 / Component handling
Pneumatic assembly stations
Bench-mounted pneumatic equipment and a vibratory parts feeder are visible in the production room. Final tooling and station choice are confirmed against the selected bottle and closure system.
02 / Factory utilities
Water-treatment system
Stainless-steel storage, activated-carbon and quartz-sand filtration vessels, pipework and the control panel are visible in this factory utility area.
Equipment images document the facility; they do not by themselves define product specifications, production capacity or compliance for an individual order.
Before production
Fragrance direction is evaluated in a dedicated setting.
Our factory includes an organized fragrance evaluation room with material references arranged for comparison. It provides a dedicated setting for scent-direction discussions and sample evaluation before production.
The room itself is not a substitute for sample approval. Available fragrance options, formula scope and the closest practical direction for a reference scent are confirmed for each project.
- 01Define the direction
Share the reference, note profile, target customer and destination market.
- 02Compare samples
Evaluate the opening, heart, dry-down and overall character before choosing.
- 03Approve before filling
Move the confirmed fragrance direction into the final concentration and packaging specification.
Quality checkpoints
Approve what will be checked before the production order.
The exact inspection plan depends on the selected formula, bottle, pump, decoration and packaging. Define acceptance criteria in the approved specification rather than relying on general factory claims.
Formula & fill
Approved reference, fragrance concentration, appearance, fill quantity and agreed batch records.
Component compatibility
Bottle, pump, collar and cap fit, including agreed leak, spray and compatibility checks.
Decoration & pack
Artwork placement, color, label or print quality, finish, carton and assembly against approved samples.
Final inspection
Agreed sampling level, count, visual checks, retained reference samples and third-party inspection when arranged.
Our factory documentation
Verify full documents privately.
Our factory maintains third-party-audited quality management documentation, including ISO 22716:2007 cosmetics GMP guidance and an SGS-audited system against FDA CFSAN Cosmetics GMP Guidelines (2008).
Public previews are intentionally and irreversibly blurred. Certificate numbers, signatures, verification codes, company details and full document text are not published.
Request current full copiesRegistration, listing or management-system certification does not constitute government approval of an individual finished product. Applicable documents are confirmed per project and destination market.
Protected previewISO 22716:2007
Cosmetics good manufacturing practice management guidance.
Protected previewSGS-Audited GMP System
Audited against FDA CFSAN Cosmetics GMP Guidelines (2008).
Documentation is project-specific
Ask for the files relevant to your destination.
A factory certificate and a finished-product document serve different purposes. Sales will clarify what is available and what may need to be prepared for the selected project.
| Management-system documents | Factory-level evidence such as current audited cosmetics GMP or ISO documentation. |
|---|---|
| Formula and product files | Availability depends on the selected fragrance, product format and commercial agreement. |
| Transport documents | Requirements vary because perfume commonly contains alcohol and may be regulated for transport. |
| Label review inputs | Destination country, language, responsible-party details and final claims affect the required content. |
| Verification | Qualified buyers should review current full files, validity dates and applicable scope before relying on them. |
Destination-market planning
Compliance is confirmed for the product and market—not assumed from one certificate.
The buyer, responsible party or importer may retain legal obligations. Before production, confirm which party owns each filing, assessment, label and post-market responsibility.
Responsible Person & product file
Confirm the EU Responsible Person, safety assessment/CPSR, PIF, CPNP notification and destination-language label review before placing the cosmetic on the market.
MoCRA scope & labeling
Confirm the responsible person, applicable facility-registration and product-listing duties, safety substantiation and label review. Registration or listing is not FDA product approval.
Importer & local registration
Confirm importer details, local notification or registration, language, ingredient restrictions, claims and transport requirements for the destination.
Project checkpoint: tell sales the destination country at the start. ARQUENOR can confirm available inputs and documents, but market access and legal responsibility must be assigned and verified for the specific finished product.
Verify before ordering
Review the factory evidence relevant to your project.
Tell us the destination country, product route and estimated quantity so we can identify the relevant current documents and quotation inputs.