ORI Bionature SDN BHD

5 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• NCONTACT3 refused lines

  No U.S. adverse event contact on supplement label

  The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

• NUTRIT LBL3 refused lines

  Nutrition information missing from label

  The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about ORI Bionature SDN BHD

Is ORI Bionature SDN BHD on an FDA import alert?

No listing for ORI Bionature SDN BHD appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Malaysia page.

Has FDA refused shipments from ORI Bionature SDN BHD?

Yes. FDA refused 3 shipment lines from ORI Bionature SDN BHD on January 30, 2017. The most recent, on January 30, 2017, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NCONTACT (no u.s. adverse event contact on supplement label).

Why did FDA refuse ORI Bionature SDN BHD's shipments?

The most frequent charges are NCONTACT (no u.s. adverse event contact on supplement label, 3 lines) and NUTRIT LBL (nutrition information missing from label, 3 lines).

When was ORI Bionature SDN BHD last inspected by FDA?

FDA's most recent inspection of ORI Bionature SDN BHD with a final classification is dated December 19, 2018 and was classified VAI (Voluntary Action Indicated).

What is ORI Bionature SDN BHD's FEI number?

ORI Bionature SDN BHD's FDA Establishment Identifier (FEI) is 3012605896.