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NingXia Zhongning Chunqi Wolfberry Technology Co. Ltd.

FDA import alert and refusal historyZhongwei, ChinaFEI 3011522359

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Example subjectNingXia Zhongning Chunqi Wolfberry Technology Co. Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, NingXia Zhongning Chunqi Wolfberry Technology Co. Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 8 of its shipment lines between July 29, 2021 and July 17, 2024, 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
Chinese red date (jujubes, ziziphus jujuba), dried or paste · FILTHY
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for NingXia Zhongning Chunqi Wolfberry Technology Co. Ltd.

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

2024

  1. Import refusal
    Refused, 2 lines in one entry: Chinese red date (jujubes, ziziphus jujuba), dried or pasteFILTHYEntry 8UU-0025574-5Show 2 lines
    • Refused, Chinese red date (jujubes, ziziphus jujuba), dried or pasteFILTHYEntry 8UU-0025574-5Source
    • Refused, Chinese red date (jujubes, ziziphus jujuba), dried or pasteFILTHYEntry 8UU-0025574-5Source
    Source
  2. Import refusal
    Refused, Chinese red date (jujubes, ziziphus jujuba), dried or pasteFILTHYEntry 8UU-0025180-1
    Source
  3. Import refusal
    Refused, Chinese red date (jujubes, ziziphus jujuba), dried or pasteFILTHYEntry 8UU-0022816-3
    Source

2023

  1. Import refusal
    Refused, Chinese red date (jujubes, ziziphus jujuba), dried or pasteFILTHYEntry 8UU-0017355-9
    Source
  2. Import refusal
    Refused, Chinese red date (jujubes, ziziphus jujuba), dried or pasteFILTHYEntry 8UU-0017219-7
    Source

2021

  1. Import refusal
    Refused, Chinese red date (jujubes, ziziphus jujuba), dried or pasteFILTHYEntry 8UU-0006657-1
    Source
  2. Import refusal
    Refused, Chinese red date (jujubes, ziziphus jujuba), dried or pasteFILTHYEntry 8UU-0006374-3
    Source

2018

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

Refusal charges, in plain English

  • FILTHY8 refused lines

    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.

Questions about NingXia Zhongning Chunqi Wolfberry Technology Co. Ltd.

Is NingXia Zhongning Chunqi Wolfberry Technology Co. Ltd. on an FDA import alert?
No listing for NingXia Zhongning Chunqi Wolfberry Technology 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 NingXia Zhongning Chunqi Wolfberry Technology Co. Ltd.?
Yes. FDA refused 8 shipment lines from NingXia Zhongning Chunqi Wolfberry Technology Co. Ltd. between July 29, 2021 and July 17, 2024. The most recent, on July 17, 2024, was chinese red date (jujubes, ziziphus jujuba), dried or paste, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse NingXia Zhongning Chunqi Wolfberry Technology Co. Ltd.'s shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 8 lines).
When was NingXia Zhongning Chunqi Wolfberry Technology Co. Ltd. last inspected by FDA?
FDA's most recent inspection of NingXia Zhongning Chunqi Wolfberry Technology Co. Ltd. with a final classification is dated August 9, 2018 and was classified VAI (Voluntary Action Indicated).
What is NingXia Zhongning Chunqi Wolfberry Technology Co. Ltd.'s FEI number?
NingXia Zhongning Chunqi Wolfberry Technology Co. Ltd.'s FDA Establishment Identifier (FEI) is 3011522359.

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Example subjectNingXia Zhongning Chunqi Wolfberry Technology 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.