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QSP Food Ingredient Co., Ltd.

FDA import alert and refusal historyShanghai, ChinaFEI 3007514108

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Example subjectQSP Food Ingredient Co., Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, QSP Food Ingredient Co., Ltd. (Shanghai, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for carrots dried, published by FDA on January 8, 2013, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for QSP Food Ingredient Co., Ltd.

1 record, newest first. Each line links to the FDA page it came from.

2013

  1. Import alert listing
    Listed on Import Alert 99-08red listCarrots Dried
    Source

Questions about QSP Food Ingredient Co., Ltd.

Is QSP Food Ingredient Co., Ltd. on an FDA import alert?
Yes. As of October 26, 2026, QSP Food Ingredient Co., Ltd. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for carrots dried; FDA published the listing on January 8, 2013.
Has FDA refused shipments from QSP Food Ingredient Co., Ltd.?
No FDA import refusals for QSP Food Ingredient Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is QSP Food Ingredient Co., Ltd.'s FEI number?
QSP Food Ingredient Co., Ltd.'s FDA Establishment Identifier (FEI) is 3007514108.
Can shipments from QSP Food Ingredient Co., Ltd. still enter the U.S.?
Shipments of carrots dried from QSP Food Ingredient Co., Ltd. can be detained without physical examination under Import Alert 99-08; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectQSP Food Ingredient 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.