Due diligence · Evidence before claims
Five-product OEM readiness matrix
This page states what is confirmed, what is conditional and what is not yet evidenced. It is not a certificate library and does not convert an Aimo statement into independent proof.
Canonical company role
Guangzhou Aimo Pet Products Co., Ltd. is the public pet-care brand, commercial and export counterparty. Its exact manufacturing partner/entity, production site and scope must be disclosed and evidenced for each project before a buyer approves production.
Readiness by category
| Category | Confirmed public-safe facts | Conditional / evidence required | Do not infer |
|---|---|---|---|
| Ear care | Non-medicated positioning; liquid MOQ ~3,000/SKU on stock bottle; wipes MOQ ~10,000 packs/SKU; qualified sample policy and 7–10 day target with boundaries. | Producing entity/site; dual-format production scope; exact formula; tests; batch documents; professional formats. | That Aimo legal entity owns both lines, is ISO 22716 certified, or every SKU includes every report. |
| Pet wipes | Commercial interest in body, paw, ear and dental formats; wipe MOQ ~10,000 packs/SKU as a commercial policy. | Converting site, substrate composition, special sachets, seal integrity, finished-wipe tests, sustainability wording. | Biodegradable/compostable/hypoallergenic/antimicrobial or in-house production without exact evidence. |
| Dog oral care | Development concept; xylitol excluded from proposed direction. | Producer and paste/wipe line; finished formula; oral-contact review; flavour; palatability; tests; pack compatibility; MOQ. | A finished enzymatic formula, guaranteed swallow safety, plaque/gingivitis efficacy or fixed MOQ. |
| Paw & nose care | Development concept for foam, wipes and conditional balm. | Balm process, producer, formula, hot/cold stability, leakage, pack compatibility, claim support and MOQ. | Verified in-house balm production, absolute lick safety, healing or protection efficacy. |
| Professional concentrates | Feasibility program for professional buyers. | Dilution ratio, final-use pH, hard-water behaviour, preservation, performance, producer, bulk pack, freight model and MOQ. | A finished 16:1/32:1 product, same-batch retail/bulk fill or superior landed cost. |
Universal buyer evidence request
1. Contracting-party licence and exact English name
2. Producing-entity licence, address and relationship
3. Process/line scope for the exact dosage form
4. GMP/certificate holder, scope and validity
5. Approved formula/specification and change control
6. Exact-SKU test plan, reports and acceptance criteria
7. Released batch COA, traceability and retained samples
8. Market responsibility matrix for brand, producer and importer
Evidence hierarchy: regulator/standard → identified certificate or lab report → controlled internal record → authorized case → independent directory/media → company marketing statement. A lower level cannot upgrade itself into a certificate or regulatory approval.