CC0 PUBLIC RECORD GRAPH Every score & timeline item links directly to its underlying U.S. FDA record (openFDA, ORA FOIA Reading Room, DECRS & OASIS).
Scoring Formula v2.0 & Legal Guardrails REST API v1
FG
GMPGraphv2.0
Global FDA Facility Graph & Co-Packer Intelligence
Facility Graph → Dietary Supplements → Sunbelt Botanicals & Capsule Manufacturing Corp.
INDEXABLE (PASSES DATA-SUFFICIENCY GATE)
Dietary Supplements FEI: 3011094827 DUNS: 051928374 🛡️ LEVEL 3 · INSPECTED & ACCEPTABLE (EMERALD SHIELD)

Sunbelt Botanicals & Capsule Manufacturing Corp.

Registered Address: 11400 NW 36th Ave, Miami, FL 33167 (United States)

For Brand Buyers: Sunbelt Botanicals & Capsule Manufacturing Corp. ranks in the top tier (A · 87/100) of Dietary Supplements establishments with LEVEL 3 · INSPECTED & ACCEPTABLE (EMERALD SHIELD). Standard quality agreement and lot-by-lot CofA verification apply.
Connected FDA Sources (1): GMPGraph Verified Co-Packer Registry & Inspection Link · Resolved Name Aliases: Sunbelt Botanicals & Capsule Manufacturing Corp.
A
87/100
Clean Record
7-Dim FDA Record Index v2.0
Fewer FDA citations than 67% of tracked Dietary Supplements facilities.
Based strictly on public U.S. FDA records as of 2026-11-03. See Formula v2.0
Dim 1 · Credit Grade
A (87/100)
Recency-Weighted Index
Dim 2 · Inspection Shield
Level 3 / 4
Physically Inspected by FDA — Acceptable Compliance Posture
Dim 4 · 'Elsa' Audit Odds
22%
LOW IMMEDIATE AUDIT PROBABILITY (Routine Cycle)
Dim 5 · 180d WL Escalation
4%
483 → Warning Letter Risk
Dim 6 · Brand Contagion
28 Brands
~119 Downstream SKUs
🛡️ Run AI Mock Inspection on This Plant ⚖️ Compare Side-by-Side vs. Clean Co-Packers 📄 Request EIR via FOIA
Represent this facility? Claim profile or post 483 closeout response (Free)
VERIFIED CONTRACT MANUFACTURER / CO-PACKER

Co-Packing Capabilities, Minimums & Certifications

Request Quote from Sunbelt Botanicals & Capsule Manufacturing Corp. →

Amazon, Shopify, and practitioner supplement brands seeking fast-turn capsule, tablet, and greens powder runs.

Minimum Run (MOQ)2,500 units
Typical Turnaround5–8 weeks
In-House Analytical LabYes (FTIR/HPLC/Micro)
Turnkey R&D FormulationAvailable
Dosage & Product Formats:
Vegan Pullulan & HPMC CapsulesTablets & Enteric SoftgelsProtein & Greens TubsEffervescent Tablets
Registrations & Quality Certifications:
21 CFR Part 111 RegisteredUL cGMP CertifiedUSDA OrganicNon-GMO Project Verified
LAYER 4 · AI BUYER DUE-DILIGENCE INTERVIEW SCRIPT Tailored to FEI 3011094827's FDA Record

5 Questions to Ask Sunbelt Botanicals & Capsule Manufacturing Corp. 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:

  1. Q1: 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?
  2. Q2: Will you sign our Quality Agreement Rider requiring 24-hour notification if an FDA investigator issues a Form 482 or Form 483 at FEI 3011094827?
  3. Q3: Can we review a redacted Master Manufacturing Record (MMR) and Batch Production Record (BPR) with dual-operator weight verification and yield reconciliation?
  4. Q4: What is your current quarantined finished-product release turnaround for USP microbial limits (<2021>/<2022>) and heavy metals (<2232>)?

Cross-Database Regulatory & Inspection Timeline

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

FDA Inspection Classification: VAI · 2025-10-14
Project Area: Dietary Supplements · Lead Investigator: Marcus V. Delgado
FDA Inspection Classification: NAI · 2023-09-22
Project Area: Dietary Supplements · Lead Investigator: Marcus V. Delgado

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) 90/100
Materials & Incoming Identity 88/100
Production & Batch Records 89/100
Facilities, Sanitation & Pest 91/100
Laboratory & Stability Controls 88/100
Packaging & Allergen Labeling 92/100
Layer 6 · Clean-Record Sourcing Alternatives

Verified AAA/AA Co-Packers in This Sector

Compare or request quotes from top-rated contract manufacturers with clean FDA inspection histories:

Lone Star Nutraceuticals & Gummy Works LLC (TX)
Grade AAA · 99/100 Clean Record
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Score Provenance Receipts

Every point in this facility's FDA Record Index (87/100) is backed by a linked government record (36-month half-life decay).

Event Date Weight Receipt
Inspection Outcome (VAI) 2025-10-14 -7.8 pts INSP-3011094827-20251014 ↗
Clean Inspection (NAI) 2023-09-22 +2.4 pts INSP-3011094827-20230922 ↗