Donglim Seafood Corporation
FDA import alert and refusal historyInchon, South KoreaFEI 3008745234
As of October 26, 2026, Donglim Seafood Corporation (Inchon, South Korea) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for capelin roe; flying fish roe, published by FDA on July 22, 2014, 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 16-120 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Donglim Seafood Corporation
2 records, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 16-120red listCapelin Roe; Flying Fish RoeSource
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about Donglim Seafood Corporation
- Is Donglim Seafood Corporation on an FDA import alert?
- Yes. As of October 26, 2026, Donglim Seafood Corporation is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for capelin roe; flying fish roe; FDA published the listing on July 22, 2014.
- Has FDA refused shipments from Donglim Seafood Corporation?
- No FDA import refusals for Donglim Seafood Corporation appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Donglim Seafood Corporation last inspected by FDA?
- FDA's most recent inspection of Donglim Seafood Corporation with a final classification is dated March 18, 2014 and was classified OAI (Official Action Indicated).
- What is Donglim Seafood Corporation's FEI number?
- Donglim Seafood Corporation's FDA Establishment Identifier (FEI) is 3008745234.
- Can shipments from Donglim Seafood Corporation still enter the U.S.?
- Shipments of capelin roe; flying fish roe from Donglim Seafood Corporation can be detained without physical examination under Import Alert 16-120; 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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