Supplier due-diligence record

FDA Supplier Evidence Snapshot

Turn a live Import Alert Radar result into a dated, source-linked record you can retain with your supplier review.

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Selected FDA firm

NUSPOWER GREATSUN (GUANGDONG) BIOTECHNOLOGY CO., LTD

China

Red list

Red-list alerts

Green-list alerts

Yellow-list alerts

2026-10-22

Dataset checked

Live preview of matched records

REDIA 66-41
04/04/2018
Detention Without Physical Examination of Unapproved New Drugs Promoted In The U.S.
Official FDA record ↗

Your delivered record includes

Exact firm name and country used for the FDA match.
Current Red / Green / Yellow List finding and every matched import alert.
Firm-entry dates, official FDA source links and dataset timestamp.
Re-checked against the official FDA page on the day it is prepared. The firm match and PDF are reviewed before delivery by email within one business day of payment.

Historical sample · 7 Oct 2026

One firm. One alert. A specific product scope.

An extract from our published PDF, not a current supplier check or a record of your supplier.

Firm in the sample

Nutrakey Industries Inc.

China · B 2403, NO 2 Minjianglu, Qingdao, Shandong

Red list · Import Alert 45-06

Detention Without Physical Examination (DWPE) for covered products.

Alert scope: Stevia leaves, crude stevia extracts and foods containing stevia leaves or extracts.
Product entries in the PDF: Includes “Natural Extract or Flavor, N.E.C.” and “All Other Products, Non-Nutritive Sweeteners”. Check the full PDF and source for all entries.
FDA firm-entry date: 13 June 2016
Sample prepared: 7 Oct 2026 · 19:19 UTC
Official source for this alert: FDA Import Alert 45-06 ↗The live source may differ from this historical sample.

Does this match your shipment?

Same name, different firm? A name alone is not confirmation. Match the country and address to your supplier documents. The sample found no other similar names in its dataset; that is not proof that homonyms do not exist.

Different product? Coverage is not established by the firm name. Compare your product and product code with the FDA entry and alert scope. This is not a universal prohibition or clearance for every product from the firm.

First page of the historical sample PDF.

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Two pages · free · no email required.

Your $24.50 snapshot is checked against the official FDA source on the day it is prepared. The firm match and PDF are reviewed before delivery. Informational evidence, not FDA certification or legal advice.