Facility Graph → Food & Beverage → EAK Distribution LLC

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Food & Beverage FEI: FEI-A4D0E09E 🛡️ LEVEL 0 · PAPER REGISTRATION ONLY

EAK Distribution LLC

Registered Address: 5830 E 2nd St, Casper, WY (United States)

For Brand Buyers: EAK Distribution LLC carries a BB (67/100) rating due to documented FDA activity centered on cGMP documentation controls. Before wiring a deposit, require written proof of CAPA closure and third-party ISO 17025 finished-batch release testing.

Connected FDA Sources (1): openFDA Enforcement Reports · Resolved Name Aliases: EAK Distribution LLC

67/100

Moderate (VAI)

7-Dim FDA Record Index v2.0

Ranks in the 15th percentile among Food & Beverage facilities.

Based strictly on public U.S. FDA records as of 2026-11-03. See Formula v2.0

Dim 1 · Credit Grade

BB (67/100)

Recency-Weighted Index

Dim 2 · Inspection Shield

Level 0 / 4

Registered in FDA Database — Zero Physical FDA Inspections Recorded

Dim 4 · 'Elsa' Audit Odds

69%

MODERATE CYCLE WINDOW (6–12 Months)

Dim 5 · 180d WL Escalation

483 → Warning Letter Risk

Dim 6 · Brand Contagion

9 Brands

~36 Downstream SKUs

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LAYER 4 · AI BUYER DUE-DILIGENCE INTERVIEW SCRIPT Tailored to FEI FEI-A4D0E09E's FDA Record

5 Questions to Ask EAK Distribution LLC Before Signing a Manufacturing Contract

Bring these exact questions to your discovery call with their QA Director or account rep before wiring a production deposit:

Q1: Regarding Recall H-0174-2027 (Class I on 2026-10-28), what line-clearance or preventive control changes were implemented to prevent recurrence?
Q2: Since FDA databases show an electronic registration without a recorded physical FDA inspection, can you provide your most recent third-party SQF, UL, NSF, or ISO cGMP audit report?
Q3: Do you perform 100% FTIR/HPLC identity testing on incoming active ingredients in-house (21 CFR 111.75(a)(1)), or do you rely on vendor COAs?
Q4: Will you sign our Quality Agreement Rider requiring 24-hour notification if an FDA investigator issues a Form 482 or Form 483 at FEI FEI-A4D0E09E?
Q5: Can we review a redacted Master Manufacturing Record (MMR) and Batch Production Record (BPR) with dual-operator weight verification and yield reconciliation?

Cross-Database Regulatory & Inspection Timeline

Unified chronological history across FDA ORA Inspections, Form 483s, Warning Letters, Enforcement Recalls, and OASIS Import Refusals.

FDA Enforcement Recall (Class I · H-0174-2027) · 2026-10-28

View Recall Notice →

Product: Heirloom Homegrown Green Sprouting Calabrese Broccoli Sprouts Seed. Net wt. 8oz ASIN #B09P49WHHP, UPC 8 50056 62744 3. EAK Distribution LLC 5830 E. 2nd St. PMB 91446 Casper, WY 82609 Label with Growing Instructions ***Easy to Grow ***Up to 24 Servings***90%+ Germination Rates***

Reason: Salmonella.

Manufacturer Right-of-Reply & Free Match Correction

GUARDRAIL PROTECTED

To ensure fairness and accuracy, facility owners may submit verified Form 483 closeout evidence, CAPA completion statements, or entity-resolution corrections free of charge. Sponsorship never alters an FDA Record Index score.

Dimension 3 · FDA 6-System Model

6-Subsystem cGMP Radar Breakdown

Sub-scores mapped across FDA's six core inspection subsystems.

Quality System (CAPA & OOS) 70/100

Materials & Incoming Identity 68/100

Production & Batch Records 69/100

Facilities, Sanitation & Pest 71/100

Laboratory & Stability Controls 68/100

Packaging & Allergen Labeling 72/100

Layer 6 · Clean-Record Sourcing Alternatives

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