
HAIOS BIOTECH supplies supplements manufactured to GMP-compliant standards in Guangzhou, China. Our company holds U.S. FDA Food Facility Registration No. 18340473528, and a COA (Certificate of Analysis) is issued for every batch. FDA registration is a facility registration — it is not an FDA approval.
| Registered entity / 注册主体 | Guangzhou Haios Biotechnology Co., Ltd. |
| Brand / 品牌 | HAIOS BIOTECH |
| FDA registration no. | 18340473528 (facility registration) |
| Facility / 工厂 | Guangzhou, China |
| Manufacturing standard | cGMP-compliant practices, QC from raw material intake to finished batch release |
| Batch documentation | COA per batch |
| Export documents | COA, MSDS, health certificate, proforma invoice, packing list |
| Markets served / 出口市场 | United States, United Kingdom, Canada, Australia, South Africa |
| Factory visits | Welcome — contact us in advance to arrange a tour |
| Response time | Replies within 12 hours |
FDA Food Facility Registration Confirmation — issued by our U.S. registration agent (Shenzhen OUA Testing Technology Co., Ltd.). The U.S. FDA does not issue or recognize certificates of registration; this document is a third-party confirmation that our company's facility registration is active. Click the image to open the full-size file.
| Registration number | 18340473528 |
| Registered entity | Guangzhou Haios Biotechnology Co., Ltd. |
| Company address | Room B514, Floor 10, Building A, 2531 Airport Road, Baiyun District, Guangzhou City |
| U.S. Registration Agent | UGK-LVM UNITED INC. |
| D-U-N-S Number | 723784541 |
| Issued | 10/14/2024 |
| Valid until | 12/31/2026 |
| Issuing body | Shenzhen OUA Testing Technology Co., Ltd. — a U.S. registration agent, not the U.S. FDA |
| What it is | A food facility registration held by our company under the U.S. FDA |
| What it is not | It is not an approval or certification of our products, our formulas or our label claims |
Our QC follows GMP practices from raw material intake through production to finished batch release, with a COA issued per batch. We describe production as running to cGMP-compliant standards and do not claim third-party certification: we publish the registration number above, and we share current documents on request instead of quoting certificate numbers we do not hold.
An analysis certificate is issued for every production batch and released with the goods.
Identity, assay, appearance, heavy metals and microbiological limits, per product specification.
COA, MSDS, health certificate, proforma invoice, packing list and other documents required for customs clearance.
We support buyers with the documentation needed for the destination market, including COA, ingredient information and testing reports. Product registration is completed by the importer or brand owner, and we cooperate fully during the process.
| Dosage forms | Hard capsules, softgels, gummies, tablets, drops, powders |
| Minimum order | 200 pcs per product |
| Sampling | 72 hours |
| Testing | COA issued per batch |
| Production | 3-5 business days (up to 200 pcs) · 5-7 business days (up to 500 pcs) |
| Shipping | 5-10 days (FOB, CIF or DDP) |
Tell us the product or formula and your destination market by WhatsApp or email.
We reply within 12 hours with the COA format, MSDS and health certificate sample for review.
Check the documents against your market requirements, then place a sample or trial order.
Buyers comparing supplement manufacturers in China can request our capability and documentation pack.
No. The U.S. FDA does not approve dietary supplement manufacturers, products or claims. Our company holds U.S. FDA Food Facility Registration No. 18340473528, which is a registration rather than an approval.
It registers our Guangzhou facility with the U.S. FDA as a food facility. It does not certify individual products, and it is not a product approval.
Yes. Send us the product name and your target market, and we will share the COA format, MSDS and health certificate sample for review. We reply within 12 hours.
We support buyers with the documentation needed for the destination market, including COA, ingredient information and testing reports. Product registration is completed by the importer or brand owner, and we cooperate fully during the process.
Tell us the product and your target market — we reply within 12 hours with the documentation you need.