Blue Ocean Co., Ltd
FDA import alert and refusal historyQuang Ngai, VietnamFEI 3006700082
Recorded by FDA as BLUE OCEAN CO., LTD
As of October 26, 2026, Blue Ocean Co., Ltd (Quang Ngai, Vietnam) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for mahi mahi, published by FDA on April 1, 2022, is also listed on Import Alert 16-81 (red list), 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 16-105 · red listIA 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Blue Ocean Co., Ltd
2 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 16-105red listMahi MahiSource
2009
- Import alert listingListed on Import Alert 16-81red listTuna (Albacore, Yellowfin, Bluefin, Skipjack, Etc.); Tuna (Albacore, Yellowfin, Bluefin, Skipjack, etc.), Hot Smoked, Fish; Tuna (Albacore, Yellowfin, Bluefin, Skipjack, etc.), Cold Smoked, FishSource
Questions about Blue Ocean Co., Ltd
- Is Blue Ocean Co., Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Blue Ocean Co., Ltd is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for mahi mahi; FDA published the listing on April 1, 2022.
- Has FDA refused shipments from Blue Ocean Co., Ltd?
- No FDA import refusals for Blue Ocean Co., Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Blue Ocean Co., Ltd's FEI number?
- Blue Ocean Co., Ltd's FDA Establishment Identifier (FEI) is 3006700082.
- Can shipments from Blue Ocean Co., Ltd still enter the U.S.?
- Shipments of mahi mahi from Blue Ocean Co., Ltd can be detained without physical examination under Import Alert 16-105; 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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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.