Soc Trang, Mekong Delta, Vietnam (VN)FEI: 3012984019DUNS: 558102944Seafood, Shrimp & Cold-Chain Aquaculture

Mekong Delta Aqua Shrimp Processing Corp.

Raw CBP/OASIS Entity String: MEKONG DELTA AQUA SHRIMP PROCESSING CORP.

FSVP Lead Auditor Note: Large IQF peeled vannamei shrimp and cooked cocktail shrimp processor in Soc Trang. Placed on Import Alert 16-81 and 16-39 Red Lists after Miami and Los Angeles FDA labs isolated Salmonella Weltevreden and Listeria monocytogenes in retail bags.

Primary US Port

Miami

Last FDA Inspection

2026-02-27

OAI (Official Action Indicated)

Detained Cargo Value

$475,500

Across 3 holds

Est. US Containers/Yr

~260 TEUs

CBP ACE Bill of Lading

Composite Procurement RiskCRITICAL_IMPORT_ALERT

100/ 100 Risk Score

5-Year Import Refusals:3

Active Warning Letters:1

FDA Enforcement Recalls:1

Red List — Import Alert 16-81 & 16-39 (Salmonella & Listeria DWPE)

Shipment Held? Request 24h Legal Review

6-Month Port Detention vs. Cleared Entry Velocity (Miami)

Source: CBP ACE Manifest + FDA OASIS Refusal Feed

May 2026

5 Held15 Cleared

Hold Rate: 25%

Jun 2026

7 Held12 Cleared

Hold Rate: 37%

Jul 2026

6 Held14 Cleared

Hold Rate: 30%

Aug 2026

5 Held13 Cleared

Hold Rate: 28%

Sep 2026

8 Held10 Cleared

Hold Rate: 44%

Oct 2026

6 Held12 Cleared

Hold Rate: 33%

Dataset 1 of 3 • FDA OASIS Import Refusals

Historical Port Detentions & Refusal Dispositions (3)

Entry # & Date	Port	Detained Product & FDA Code	Charge Code & Import Alert	Cargo Value	Final CBP/FDA Disposition
M52-7710294-8 2026-09-19	Miami	IQF Cooked Peeled & Deveined Tail-On White Shrimp (2lb Retail Bags) FDA Product Code: 16J	LISTERIA Import Alert 16-39	$184,000	Refused & Exported
M52-7591022-1 2026-06-04	Miami	Raw Headless Shell-On Vannamei Shrimp 16/20 (10x4lb Master Cartons) FDA Product Code: 16J	SALMONELLA Import Alert 16-81	$162,500	Detained Pending Lab Packet
W94-8391044-7 2025-12-18	Los Angeles	Frozen Breaded Butterfly Coconut Shrimp FDA Product Code: 16K	FILTH Import Alert 16-18	$129,000	Refused & Exported

Dataset 2 of 3 • CDER / CFSAN / CDRH Enforcement

FDA Warning Letters & Form 483 Citations (1)

CMS-674910 • Issued 2026-04-09Active / Open

CFSAN Division of Seafood Safety

Serious Deviations from Seafood HACCP Regulation (21 CFR Part 123)

Critical Control Point (CCP) cooking step logs lacked continuous temperature chart verification, and post-cook IQF tunnel belts tested positive for Listeria spp.

21 CFR § 123.6(c)21 CFR § 123.11FD&C Act § 402(a)(4)

Dataset 3 of 3 • RES Recall Enterprise System

5-Year US Market Recalls (1)

Recall #F-0619-2026 (2026-05-02)Class I

Pacific Ring Ready-to-Eat Cooked Cocktail Shrimp Ring w/ Sauce (16 oz)

Reason: Potential contamination with Listeria monocytogenes in post-lethality glazing line.

Distribution Scope: 24,000 trays (Southeast US grocery chains)

Plain-English Statutory Translation & Importer Action Plan

Cited FDA Charge Codes & Remediation Checklists for Mekong Delta Aqua Shrimp Processing Corp.

LISTERIA (FD&C Act Section 402(a)(1))Form 766 Ineligible (Lab/Export)

Adulterated: Bears or contains Listeria monocytogenes

Ready-to-eat (RTE) seafood, dairy, or botanical extract tested positive or is subject to DWPE for Listeria monocytogenes, a high-fatality foodborne pathogen.

Importer Remediation Checklist:

Immediately quarantine co-mingled lots and commission AOAC/BAM Listeria monocytogenes cultural confirmation.
Audit cold-chain and post-lethality environmental swab logs (Zones 1-3) from the overseas processing facility.
Coordinate with US customs broker and FDA compliance counsel to hold liquidation while private laboratory packets are reviewed by FDA Division Compliance.

Typical Hold: 25–42 calendar daysView Full LISTERIA Form 766 Playbook →

SALMONELLA (FD&C Act Section 402(a)(1))Form 766 Ineligible (Lab/Export)

Adulterated: Appears to contain Salmonella, a poisonous and deleterious substance

FDA microbiological sampling or Import Alert 99-19 / 16-81 surveillance flagged the food, spice, or aquaculture shipment for Salmonella spp. contamination.

Importer Remediation Checklist:

Engage an FDA-recognized private laboratory for BAM Chapter 5 Salmonella composite composite testing (15 to 60 subsamples depending on lot risk).
Do not attempt Form FDA 766 relabeling; pathogen-adulterated food requires an approved heat-treatment/irradiation reconditioning protocol or export/destruction.
Prepare a Root Cause Analysis (RCA) and 5 consecutive non-violative commercial shipment packets to petition off Import Alert Red List.

Typical Hold: 24–40 calendar daysView Full SALMONELLA Form 766 Playbook →

FILTH (FD&C Act Section 402(a)(3))Form 766 Ineligible (Lab/Export)

Adulterated: Consists in whole or in part of filthy, putrid, or decomposed substance

FDA port inspectors or laboratory analysis detected insect fragments, rodent hair, mold, or decomposition in the shipment.

Importer Remediation Checklist:

Commission an accredited independent 3rd-party lab micro-filth analysis within 10 business days of Notice of FDA Action.
Submit a Petition for Removal from Detention Without Physical Examination (DWPE) after 5 consecutive clean shipments.
Audit factory HACCP sanitation records before wiring balance payments.

Typical Hold: 21–35 calendar daysView Full FILTH Form 766 Playbook →

TIER 2 • PROCUREMENT DATA & REAL-TIME OASIS WEBHOOK MONITORFEI #3012984019 • Instant Delivery

5-Year Cleaned Excel Pack$39 One-Time

Download Normalized 5-Year Refusal, 483 & Recall Audit Workbook (.XLSX + CSV)

Includes all deduplicated overseas factory names, FEI/DUNS crosswalks, 5-year port refusal logs, plain-English statutory violation mappings, and FSVP supplier qualification templates ready for customs broker review.

Full 5-year OASIS refusal history for Mekong Delta Aqua Shrimp Processing Corp. + category peers
21 CFR 1.505 Foreign Supplier Verification Program (FSVP) audit checklist tab

Buy Cleaned 5-Yr Excel ($39)PayPal.me ($39)

⬇ Download Audit Sample (.XLS Workbook)⬇ Download Audit Sample (UTF-8 .CSV)

FEI #3012984019 Watchdog$15 / month

Instant Supplier Detention Webhook & Email Alert Monitor

Get an automated Slack/Webhook JSON payload and email alert within 15 minutes whenever FDA OASIS logs a new detention, Import Alert Red List addition, or Warning Letter for Mekong Delta Aqua Shrimp Processing Corp. before you wire your 70% balance payment.

TIER 3 • URGENT US FDA COMPLIANCE COUNSEL DISPATCH (CPL VERIFIED)

Respond-By Deadline Priority Triage

Shipment Detained by FDA or Placed on Import Alert? Request Free 24h Detention Evaluation from Licensed US FDA Compliance Counsel

When FDA issues a Notice of FDA Action (Detention), importers typically have only 10 to 20 business days to file a Form FDA 766 relabeling application, submit an accredited private laboratory packet (PLAP), or petition for Import Alert Red List removal before CBP orders refusal and liquidated damages.

Your Full Name & Role (Required)

Include your name and title (e.g., “Sarah Chen, VP Supply Chain”).

Please provide your full name (at least 2 characters).

Work Email for 24h Legal Memo (Required)

Used strictly to deliver your conflict-free 24h FDA detention evaluation.

Please enter a valid corporate email address.

Importer Website or Amazon/Shopify Store URL (Required)

Include https:// so counsel can pre-screen product Intended Use claims.

Please enter a valid URL starting with https:// or http://.

CBP Entry Number or Supplier FEI # (Required)

Format: 10-digit FEI (e.g., 3012984019) or 11-char CBP Entry # (e.g., W94-8829104-3).

Enter a 5–24 character alphanumeric FEI number or CBP Entry number.

US Port of Detention

Select the FDA District / Port holding the cargo.

Primary Cited FDA Charge Code

Charge listed on your Notice of FDA Action.

Commercial Cargo Value at Risk

Determines Form 766 vs. PLAP economic viability.

Notice of FDA Action Summary & Respond-By Date (Optional)

Describe whether cargo is currently on hold in ITACS, whether private lab sampling has started, or if you need an Import Alert removal petition.

🔒 Confidential submission • Zero upfront cost for 24h detention evaluation • Matched with licensed US FDA / Customs attorneys.

Compare Alternative Suppliers in Seafood, Shrimp & Cold-Chain Aquaculture

View Category Detention Report →

Mazatlan Pacifico Mariscos Congelados S.A. de C.V.

Mexico • FEI 3013891022 • Red List — Import Alert 16-18 & 16-39 (Decomposition & Listeria)

75/100

Mekong Delta Aqua Shrimp Processing Corp. Compliance FAQ

Is Mekong Delta Aqua Shrimp Processing Corp. (FEI 3012984019) on an FDA Import Alert Red List?

Mekong Delta Aqua Shrimp Processing Corp. currently carries a Composite FDA Risk Score of 100/100 (CRITICAL_IMPORT_ALERT) in DWPERadar records with status: Red List — Import Alert 16-81 & 16-39 (Salmonella & Listeria DWPE). Primary US port of entry is Miami. Historical records are informational only and should be cross-checked on official FDA dashboards before CBP filing.

What are the main FDA Charge Codes cited against Mekong Delta Aqua Shrimp Processing Corp.?

Across the 5-year OASIS refusal dataset, Mekong Delta Aqua Shrimp Processing Corp. has been cited for LISTERIA, SALMONELLA, FILTH. Importers should review the statutory remediation checklists and Form FDA 766 eligibility before filing CBP entry.