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Yuxing Biotechnology (Group) Co., Ltd.

FDA import alert and refusal historyXingtai, ChinaFEI 3008996626

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Example subjectYuxing Biotechnology (Group) Co., Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Yuxing Biotechnology (Group) Co., Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 16 of its shipment lines between June 27, 2017 and August 18, 2026, most often for drug gmps (DRUG GMPS).

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

Current status

Import alerts
Not listed
Last import refusal
Hydroxocobalamin (vitamin) · DRUG GMPS
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Yuxing Biotechnology (Group) Co., Ltd.

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

2026

  1. Import refusal
    Refused, Hydroxocobalamin (vitamin)DRUG GMPSEntry AEK-9632794-3
    Source
  2. Import refusal
    Refused, Mecobalamin (vitamin)SUPPL GMPEntry AEK-0734831-0
    Source

2024

  1. Import refusal
    Refused, Vitamin b12 (cyanocobalamin)DRUG GMPSEntry AEK-4702665-1
    Source

2023

  1. Import refusal
    Refused, 8 lines in one entry: Vitamin b12 (cyanocobalamin); Mecobalamin (vitamin)DRUG GMPSEntry 024-1650269-4Show 8 lines
    Source
  2. Import refusal
    Refused, Hydroxocobalamin (vitamin)UNAPPROVEDEntry AEK-2990538-5
    Source
  3. Import refusal
    Refused, Mecobalamin (vitamin)SUPPL GMPEntry AEK-2955933-1
    Source

2019

  1. Import refusal
    Refused, Mecobalamin (vitamin)DRUG GMPSEntry AEK-6321517-9
    Source
  2. Import refusal
    Refused, Mecobalamin (vitamin)DRUG GMPSEntry AEK-5733530-6
    Source

2018

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2017

  1. Import refusal
    Refused, Hydroxocobalamin (vitamin)DRUG GMPSEntry AEK-3542261-4
    Source

2014

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ
    Source

Refusal charges, in plain English

  • DRUG GMPS13 refused lines

    DRUG GMPS

  • SUPPL GMP2 refused lines

    Dietary supplement CGMP not met

    The product appeared to be a dietary supplement prepared, packed, or held under conditions that do not meet current good manufacturing practice (CGMP) regulations.

  • 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 Yuxing Biotechnology (Group) Co., Ltd.

Is Yuxing Biotechnology (Group) Co., Ltd. on an FDA import alert?
No listing for Yuxing Biotechnology (Group) 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 Yuxing Biotechnology (Group) Co., Ltd.?
Yes. FDA refused 16 shipment lines from Yuxing Biotechnology (Group) Co., Ltd. between June 27, 2017 and August 18, 2026. The most recent, on August 18, 2026, was hydroxocobalamin (vitamin), charged as DRUG GMPS (drug gmps).
Why did FDA refuse Yuxing Biotechnology (Group) Co., Ltd.'s shipments?
The most frequent charges are DRUG GMPS (drug gmps, 13 lines) and SUPPL GMP (dietary supplement cgmp not met, 2 lines).
When was Yuxing Biotechnology (Group) Co., Ltd. last inspected by FDA?
FDA's most recent inspection of Yuxing Biotechnology (Group) Co., Ltd. with a final classification is dated May 17, 2018 and was classified VAI (Voluntary Action Indicated).
What is Yuxing Biotechnology (Group) Co., Ltd.'s FEI number?
Yuxing Biotechnology (Group) Co., Ltd.'s FDA Establishment Identifier (FEI) is 3008996626.

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Example subjectYuxing Biotechnology (Group) Co., Ltd added to Import Alert 16-129 (red list)

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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.