Pet-Supplement-OEM in China prüfen, bevor Sie fliegen
Kurzantwort
Vor der Reise: GMP- und SQF-Zertifikate mit Kennung und Daten, den Fertigungsnamen auf der Rechnung, FDA-Betriebsnummer für die USA, ein Muster-COA und eine schriftliche Musterfrist. Wer diese PDFs nicht schickt, ist nicht bereit für Ihre Marke.
Von Beno Quality Team
A factory tour is useful. It is a poor first filter. Traders book nice meeting rooms. Real OEMs send files.
If you sell into retail or a regulated import channel, the document pack is the thing that gets you onboarded, not the lunch. Run this list before anyone on your team flies to Jiangsu.
We publish the same files we send to buyers on the quality and company page. If a supplier will not match that level of evidence, keep looking.
The five files to request in the first email
Ask for PDFs, not screenshots. Screenshots hide expiry dates.
- GMP certificate with identifier, audit date and validity. Ours is Eurofins GMP audit recognition, identifier ACCB8AAA422_1, valid through 14 June 2027.
- SQF certificate for pet food manufacturing (GFSI-recognised), not a generic "ISO-style" poster. Ours is SQF Food Safety Code: Pet Food Manufacturing, Edition 9, SIN 105690.
- Legal name that will appear on the commercial invoice and packing list. Production here is Taizhou Beno Biotech Co., Ltd., Taixing, Jiangsu. If the WeChat name and the invoice name do not match, stop.
- FDA facility registration number if the US is in your plan. Ours is 10222600768. D-U-N-S 404129816 is the other identifier buyers use to confirm the entity.
- A sample COA from a recent batch of a similar format, plus a written sampling lead time (we quote 7–15 days for stock formulas).
If those five arrive complete, a visit is optional. If they arrive incomplete, a visit will not fix it.
What a video is for
A 30-second corridor clip is not evidence. You want to see gowning, a line, and packing with the same plant identity as the certificates.
We put a factory walk-through and shop-floor clips on the homepage. Watch those before you ask for a live tour. If you still want to visit, say so in the brief; we will tell you which day the line you care about is running.
Red flags that waste a quarter
- MOQ described only as "negotiable" with no format attached
- Certificates issued to a different city or a trading company
- No factory address you can drop into a map (ours is Li Kong Group 3, Donglin Village, Yaowang Street, Taixing 225400)
- Sample "in 3 days" with no formula selected
- Pressure to pay a tooling deposit before you have seen a COA
None of that means the person is lying. It means you cannot put them in front of your quality team yet.
After the files: one sample, then a quote
Do not brief five factories with a vague "joint chew, private label." Send the same short brief to two plants that passed the file check: species, benefit, format, destination market, volume band. Compare sample, COA layout, and whether the quote names Incoterm and MOQ.
When you are ready, use the quotation form. Attach the market and the format. We will tell you if it is a stock SKU at 500 units or an ODM track.
Häufige Fragen
- What certificates should a pet supplement OEM in China send before a visit?
- Ask for GMP and SQF PDFs with identifier and validity dates, the legal manufacturing name that will appear on invoices, FDA facility registration if you import to the US, and a sample COA. If those files are missing, postpone the trip.
- How do I know I am talking to the factory and not a trader?
- Match the certificate legal name to the invoice entity and to a physical plant address. Ask for a line video that matches that site. Taizhou Beno Biotech Co., Ltd. in Taixing, Jiangsu is the manufacturer behind Beno production.
- Is a factory audit still needed if certificates check out?
- Retailers and some importers still want an on-site or third-party audit. Certificates get you to that conversation. They do not replace it for every channel. Start with files so you only audit plants that can already produce your format.
Machen Sie ein Produkt daraus
Senden Sie uns ein Briefing – unser OEM/ODM-Team bestätigt Weg, MOQ und Musterprozess.
