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St. John International, S.A.

FDA import alert and refusal historyGeneva, SwitzerlandFEI 1000144431

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Example subjectSt. John International, S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, St. John International, S.A. (Geneva, Switzerland) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for frozen shrimp, published by FDA on September 16, 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 St. John International, S.A.

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

2009

  1. Import alert listing
    Listed on Import Alert 99-21red listFrozen Shrimp
    Source

Questions about St. John International, S.A.

Is St. John International, S.A. on an FDA import alert?
Yes. As of October 26, 2026, St. John International, S.A. is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for frozen shrimp; FDA published the listing on September 16, 2009.
Has FDA refused shipments from St. John International, S.A.?
No FDA import refusals for St. John International, S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is St. John International, S.A.'s FEI number?
St. John International, S.A.'s FDA Establishment Identifier (FEI) is 1000144431.
Can shipments from St. John International, S.A. still enter the U.S.?
Shipments of frozen shrimp from St. John International, S.A. can be detained without physical examination under Import Alert 99-21; 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 subjectSt. John International, S.A 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.