Baltic Shore Organization
FDA import alert and refusal historySaint Petersburg, RussiaFEI 3007914038
As of October 26, 2026, Baltic Shore Organization (Saint Petersburg, Russia) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for kilka of baltic salted small fish; herring w/olives; tsar's cuisine herring in oil w/smoke flavor; herring salted, published by FDA on October 2, 2015, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Baltic Shore Organization
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-39red listKilka of Baltic Salted Small Fish; Herring w/olives; Tsar's Cuisine Herring in Oil w/Smoke flavor; Herring SaltedSource
Questions about Baltic Shore Organization
- Is Baltic Shore Organization on an FDA import alert?
- Yes. As of October 26, 2026, Baltic Shore Organization is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for kilka of baltic salted small fish; herring w/olives; tsar's cuisine herring in oil w/smoke flavor; herring salted; FDA published the listing on October 2, 2015.
- Has FDA refused shipments from Baltic Shore Organization?
- No FDA import refusals for Baltic Shore Organization appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Baltic Shore Organization's FEI number?
- Baltic Shore Organization's FDA Establishment Identifier (FEI) is 3007914038.
- Can shipments from Baltic Shore Organization still enter the U.S.?
- Shipments of kilka of baltic salted small fish; herring w/olives; tsar's cuisine herring in oil w/smoke flavor; herring salted from Baltic Shore Organization can be detained without physical examination under Import Alert 99-39; 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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