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Nguyen Thi Kim Manh

FDA import alert and refusal historyAn Giang, VietnamFEI 3013496138

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Example subjectNguyen Thi Kim Man added to Import Alert 16-129 (red list)

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As of October 26, 2026, Nguyen Thi Kim Manh is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines on June 6, 2018, 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
Gourmay, gourami · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Nguyen Thi Kim Manh

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

2018

  1. Import refusal
    Refused, 4 lines in one entry: Gourmay, gourami; Carp, cakes, balls, etc.FILTHYEntry BED-0029626-2Show 4 lines
    Source

Refusal charges, in plain English

  • FILTHY4 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 Nguyen Thi Kim Manh

Is Nguyen Thi Kim Manh on an FDA import alert?
No listing for Nguyen Thi Kim Manh appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Vietnam page.
Has FDA refused shipments from Nguyen Thi Kim Manh?
Yes. FDA refused 4 shipment lines from Nguyen Thi Kim Manh on June 6, 2018. The most recent, on June 6, 2018, was gourmay, gourami, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Nguyen Thi Kim Manh's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 4 lines).
What is Nguyen Thi Kim Manh's FEI number?
Nguyen Thi Kim Manh's FDA Establishment Identifier (FEI) is 3013496138.

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Example subjectNguyen Thi Kim Man 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.