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Laiyang Ruifeng Food Co., Ltd.

FDA import alert and refusal historyYantaishi, ChinaFEI 3011065190

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

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As of October 26, 2026, Laiyang Ruifeng Food Co., Ltd. (Yantaishi, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for yellow pepper strips, published by FDA on March 4, 2016, 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 Laiyang Ruifeng Food Co., Ltd.

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

2016

  1. Import alert listing
    Listed on Import Alert 99-08red listYellow Pepper Strips
    Source

Questions about Laiyang Ruifeng Food Co., Ltd.

Is Laiyang Ruifeng Food Co., Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Laiyang Ruifeng Food Co., Ltd. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for yellow pepper strips; FDA published the listing on March 4, 2016.
Has FDA refused shipments from Laiyang Ruifeng Food Co., Ltd.?
No FDA import refusals for Laiyang Ruifeng Food Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Laiyang Ruifeng Food Co., Ltd.'s FEI number?
Laiyang Ruifeng Food Co., Ltd.'s FDA Establishment Identifier (FEI) is 3011065190.
Can shipments from Laiyang Ruifeng Food Co., Ltd. still enter the U.S.?
Shipments of yellow pepper strips from Laiyang Ruifeng Food 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 subjectLaiyang Ruifeng Food 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.