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Zhejiang NHU Company Ltd. (Plant 1)

FDA import alert and refusal historyShaoxing, ChinaFEI 3004347352

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Example subjectZhejiang NHU Company Ltd. (Plant 1 added to Import Alert 16-129 (red list)

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As of October 26, 2026, Zhejiang NHU Company Ltd. (Plant 1) has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on August 21, 2015, was classified VAI (Voluntary Action Indicated).

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

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Zhejiang NHU Company Ltd. (Plant 1)

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

2015

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

2012

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

Questions about Zhejiang NHU Company Ltd. (Plant 1)

Is Zhejiang NHU Company Ltd. (Plant 1) on an FDA import alert?
No listing for Zhejiang NHU Company Ltd. (Plant 1) 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 Zhejiang NHU Company Ltd. (Plant 1)?
No FDA import refusals for Zhejiang NHU Company Ltd. (Plant 1) appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Zhejiang NHU Company Ltd. (Plant 1) last inspected by FDA?
FDA's most recent inspection of Zhejiang NHU Company Ltd. (Plant 1) with a final classification is dated August 21, 2015 and was classified VAI (Voluntary Action Indicated).
What is Zhejiang NHU Company Ltd. (Plant 1)'s FEI number?
Zhejiang NHU Company Ltd. (Plant 1)'s FDA Establishment Identifier (FEI) is 3004347352.

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Example subjectZhejiang NHU Company Ltd. (Plant 1 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.