Cadovimex-II Seafood Im-Ex & Processing Joint-Stock Company
FDA import alert and refusal historySadec, VietnamFEI 3007005183
Recorded by FDA as CADOVIMEX-II SEAFOOD IM-EX & PROCESSING JOINT-STOCK COMPANY
As of October 26, 2026, Cadovimex-II Seafood Im-Ex & Processing Joint-Stock Company (Sadec, Vietnam) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for tilapia, published by FDA on July 21, 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 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 Cadovimex-II Seafood Im-Ex & Processing Joint-Stock Company
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 16-81red listTilapiaSource
Questions about Cadovimex-II Seafood Im-Ex & Processing Joint-Stock Company
- Is Cadovimex-II Seafood Im-Ex & Processing Joint-Stock Company on an FDA import alert?
- Yes. As of October 26, 2026, Cadovimex-II Seafood Im-Ex & Processing Joint-Stock Company is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for tilapia; FDA published the listing on July 21, 2015.
- Has FDA refused shipments from Cadovimex-II Seafood Im-Ex & Processing Joint-Stock Company?
- No FDA import refusals for Cadovimex-II Seafood Im-Ex & Processing Joint-Stock Company appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Cadovimex-II Seafood Im-Ex & Processing Joint-Stock Company's FEI number?
- Cadovimex-II Seafood Im-Ex & Processing Joint-Stock Company's FDA Establishment Identifier (FEI) is 3007005183.
- Can shipments from Cadovimex-II Seafood Im-Ex & Processing Joint-Stock Company still enter the U.S.?
- Shipments of tilapia from Cadovimex-II Seafood Im-Ex & Processing Joint-Stock Company can be detained without physical examination under Import Alert 16-81; 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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