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Aogubio Co Ltd

FDA import alert and refusal historyXian, ChinaFEI 3035176258

Recorded by FDA as AOGUBIO CO LTD

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Example subjectAogubio Co Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Aogubio Co Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between January 20, 2026 and June 26, 2026, most often for filthy, putrid or decomposed substance (FILTHY).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Nicotinamide (niacinamide) (vitamin) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Aogubio Co Ltd

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

2026

  1. Import refusal
    Refused, Nicotinamide (niacinamide) (vitamin)UNAPPROVEDEntry AEK-0576023-5
    Source
  2. Import refusal
    Refused, Mushrooms and other fungi products, broken or kibbled, n.e.c.FILTHYEntry SCS-3795920-8
    Source

Refusal charges, in plain English

  • FILTHY1 refused line

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

  • UNAPPROVED1 refused line

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Aogubio Co Ltd

Is Aogubio Co Ltd on an FDA import alert?
No listing for Aogubio Co Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the China page.
Has FDA refused shipments from Aogubio Co Ltd?
Yes. FDA refused 2 shipment lines from Aogubio Co Ltd between January 20, 2026 and June 26, 2026. The most recent, on June 26, 2026, was nicotinamide (niacinamide) (vitamin), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Aogubio Co Ltd's shipments?
The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 1 line) and UNAPPROVED (unapproved new drug, 1 line).
What is Aogubio Co Ltd's FEI number?
Aogubio Co Ltd's FDA Establishment Identifier (FEI) is 3035176258.

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.