Stated exactly as it is.

Safety data sheets (SDS / MSDS) prepared for the market you are selling into, the ingredient / INCI list, batch documentation on request, our FDA facility registration and product listing, CE documentation, and the SGS test report. Ask for them before you order samples: a supplier who cannot name the document will not produce it after the order either.

No. We hold FDA facility registration and product listing, CE-standard documentation and an SGS lab report - not an ISO or GMP certificate. We would rather tell you now than let it surface when your retailer asks. What we can do instead: send the documents we do hold, and welcome an audit or a walkthrough of the line in Pingdu, which is usually what a buyer asking for GMP wants to establish.

On file: CE documentation for eyelash extensions covering RoHS, plus SGS testing for heavy metals (lead against California Proposition 65, total mercury against US FDA 21 CFR - both Not Detected) and a full microbial panel. If your market or marketplace checklist names a specific EU chemical regulation, send us the checklist: we will map it line by line to what we hold and tell you plainly which lines we cannot cover today, rather than let you find out at customs.

You appoint one, and we help you do it. EU law requires a Responsible Person established inside the EU - your own company if you are EU-based, your importer, or a paid RP service, and we can tell you which of the three fits your setup. A factory in China cannot hold the role, so no supplier who offers to be your RP is describing something real. Once appointed, we deal with them directly and hand over the file they need: product composition and INCI, the safety data sheet for your market, manufacturing description, our FDA facility registration and product listing, CE documentation and the SGS test report. Your RP's name and EU address then go onto the label we print for you.

Four things, and we walk you through each. (1) A Responsible Person established in the EU - you appoint them; we tell you which option fits and brief them once they are in place. (2) A Product Information File - we supply the composition and INCI, the manufacturing description, and our compliance documents, which is most of what goes in it. (3) A Cosmetic Product Safety Report - written and signed by a qualified safety assessor, not by us; what the assessor asks for is composition, impurity and heavy-metal data and microbial results, and we hand those over, including our SGS report. (4) CPNP notification - filed by your Responsible Person; we supply the product data, packaging details and label artwork it needs. Local-language labelling with your RP's name and EU address is printed by us on the same run as your brand. Send us your market's checklist and we will mark line by line what we cover and what is yours.

We import Korean PBT and manufacture the trays in Pingdu, Qingdao, China. If you need the fibre mill named for your own supply-chain file, ask in writing and we will state the mill and batch on your quotation. We will not put a mill name against a batch we did not use, which is why it is answered per order rather than as a standing claim on a page.

Both files download from this page. The facility registration says the U.S. FDA knows who we are and where we manufacture. The product listing says the FDA knows which products we make under that registration. Neither is an approval, a clearance or a certification - the FDA does not approve or certify cosmetics, so a supplier telling you their lashes are FDA approved is describing something that does not exist.