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Della Gida San Ve Tic A.S.

FDA import alert and refusal historyIstanbul, TurkeyFEI 3009716220

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Example subjectDella Gida San Ve Tic A.S added to Import Alert 16-129 (red list)

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As of October 26, 2026, Della Gida San Ve Tic A.S. (Istanbul, Turkey) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for orange flavored soft drink, published by FDA on April 25, 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 Della Gida San Ve Tic A.S.

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

2016

  1. Import alert listing
    Listed on Import Alert 45-02red listOrange Flavored Soft Drink
    Source

Questions about Della Gida San Ve Tic A.S.

Is Della Gida San Ve Tic A.S. on an FDA import alert?
Yes. As of October 26, 2026, Della Gida San Ve Tic A.S. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for orange flavored soft drink; FDA published the listing on April 25, 2016.
Has FDA refused shipments from Della Gida San Ve Tic A.S.?
No FDA import refusals for Della Gida San Ve Tic A.S. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Della Gida San Ve Tic A.S.'s FEI number?
Della Gida San Ve Tic A.S.'s FDA Establishment Identifier (FEI) is 3009716220.
Can shipments from Della Gida San Ve Tic A.S. still enter the U.S.?
Shipments of orange flavored soft drink from Della Gida San Ve Tic A.S. 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 subjectDella Gida San Ve Tic A.S 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.