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Productora Quisqueyana Sa (Fce #)

FDA import alert and refusal historySanto Domingo, Dominican RepublicFEI 3002809201

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Example subjectProductora Quisqueyana Sa (Fce # added to Import Alert 16-129 (red list)

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As of October 27, 2026, Productora Quisqueyana Sa (Fce #) (Santo Domingo, Dominican Republic) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for guava, dried or paste, plastic, synth, commercially sterile, published by FDA on September 18, 2009, 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 Productora Quisqueyana Sa (Fce #)

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

2009

  1. Import alert listing
    Listed on Import Alert 45-02red listGuava, Dried or Paste, Plastic, Synth, Commercially Sterile
    Source

Questions about Productora Quisqueyana Sa (Fce #)

Is Productora Quisqueyana Sa (Fce #) on an FDA import alert?
Yes. As of October 27, 2026, Productora Quisqueyana Sa (Fce #) is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for guava, dried or paste, plastic, synth, commercially sterile; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Productora Quisqueyana Sa (Fce #)?
No FDA import refusals for Productora Quisqueyana Sa (Fce #) appear in FDA's refusal data since October 2016, as of October 27, 2026.
What is Productora Quisqueyana Sa (Fce #)'s FEI number?
Productora Quisqueyana Sa (Fce #)'s FDA Establishment Identifier (FEI) is 3002809201.
Can shipments from Productora Quisqueyana Sa (Fce #) still enter the U.S.?
Shipments of guava, dried or paste, plastic, synth, commercially sterile from Productora Quisqueyana Sa (Fce #) can be detained without physical examination under Import Alert 45-02; 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 subjectProductora Quisqueyana Sa (Fce # 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.