Seagarden AS

4 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• SULFITELBL2 refused lines

  SULFITELBL

Questions about Seagarden AS

Is Seagarden AS on an FDA import alert?

Yes. As of October 25, 2026, Seagarden AS is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for shrimp powder premium; FDA published the listing on May 5, 2017.

Has FDA refused shipments from Seagarden AS?

Yes. FDA refused 2 shipment lines from Seagarden AS between June 23, 2017 and August 21, 2025. The most recent, on August 21, 2025, was shrimp & prawns, cakes, balls, etc., charged as SULFITELBL (sulfitelbl).

Why did FDA refuse Seagarden AS's shipments?

The most frequent charge is SULFITELBL (sulfitelbl, 2 lines).

When was Seagarden AS last inspected by FDA?

FDA's most recent inspection of Seagarden AS with a final classification is dated September 20, 2019 and was classified NAI (No Action Indicated).

What is Seagarden AS's FEI number?

Seagarden AS's FDA Establishment Identifier (FEI) is 3009252780.

Can shipments from Seagarden AS still enter the U.S.?

Shipments of shrimp powder premium from Seagarden AS 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).