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Production-base profile
Zhuhai Yaho Biotechnology Co., Ltd. is the named legal manufacturing entity and operates the facility. Representative directions include grain-based sticks, vegetable-recipe concepts and shaped chews. The page does not claim digestibility or oral-care performance; any such positioning requires final-product evidence and destination-market review. Aumeats coordinates the international customer workstream and preliminary facility assessment but is not the site operator. Formula, process fit, current document status, capacity, packaging and market requirements are verified for the individual project.
Facility Role
Zhuhai Yaho Biotechnology Co., Ltd. is the legal manufacturing entity and site operator. Aumeats manages the overseas customer interface, product-development brief, commercial coordination, qualification-document requirements and export delivery workstream; Aumeats is not the site operator.
Region: Zhuhai, China
Zhuhai Yaho Biotechnology Co., Ltd. operates this specialist production base and participates in the Aumeats production network. Aumeats coordinates international customer requirements and allocates projects according to product, process, compliance, capacity, cost and delivery needs; it does not replace the legal manufacturing entity.
View the Aumeats Production NetworkProduct, process, market, capacity, cost and delivery requirements are reviewed before the production base is assigned.
Formula version, dimensions, texture, analytical targets, packaging and acceptance criteria are confirmed in writing.
Incoming-material, process, finished-product and batch-release evidence follows the approved project quality plan.
Labels, certificates, commercial documents and shipment milestones are coordinated for the agreed destination route.
Antler, ring, S-shape, bone and other formats. Size, hardness, intended use and suitability are confirmed for the specific project.
Bone, toothbrush, rope, spiral and multi-ridge shapes with project-specific size, flavour and hardness. Shape alone does not establish a health or performance benefit.
Vegetable-led concepts and distinctive moulded formats for merchandising ranges. Ingredient identity, formulation and any claim require project-specific review.
Aumeats manages the customer brief, sample matching, cost assessment, packaging, documents and export coordination.
The named legal entity, not Aumeats, is responsible for manufacturing operations, site controls and manufacturing records.
Aumeats is the international project coordinator and manages the customer brief, commercial communication, qualification evidence and export-delivery interface.
Forecast, change control, corrective actions and range extensions are managed through the same project interface.
Facility & Equipment
Facility photography supports preliminary customer qualification and production-capability review.
Product Range
Final formula, specification, pack format, quality plan and market eligibility are confirmed for each order.
Production Control
Confirm raw materials, formula version, additives, flavour, colour and analytical targets.
Control mixing, extrusion, mould, dimensions, weight and surface texture.
Set parameters around moisture, hardness, resilience and dimensional stability.
Check sensory, dimensions, weight, physical characteristics and agreed analysis.
Confirm seal, net weight, batch code, artwork, barcode, case pack and channel requirements.
Aumeats coordinates batch records, quality documents, inspection and export milestones.
Qualification Documents
The certificate displays 16 June 2028 as its expiry date. Current status, the named legal entity, facility address and applicable scope are verified for each project.
The document displays 10 February 2030 as its expiry date for the recorded categories. Current status and applicability are reconfirmed for each order.
A relevant registration list extract is available for controlled customer qualification. It is not presented as a general EU approval; product, facility and destination eligibility are verified before order confirmation.
The third-party document displays 31 December 2026 as its expiry date. It was not issued, recognised or approved by the U.S. FDA and does not establish FDA certification, product approval or market eligibility. Current status is independently verified during customer qualification.
Facility Project Brief
Send the target market, benchmark or specification, expected volume, packaging, quality requirements and required delivery date. Aumeats will confirm whether this base is the appropriate production route.