AIDEVI laboratory reports and manufacturing standards
AIDEVI Quality Evidence Library

Lab Reports & Manufacturing Standards

Learn how AIDEVI documents manufacturing standards, third-party testing, and batch-level quality records for selected products.

Certification Overview

Evidence organized for easier review.

The records below represent different parts of AIDEVI's quality and manufacturing framework. Certification scope, availability, and relevance may vary by facility, product, and batch.

NSF GMP certification mark
GMP Standard

NSF GMP Certification

Certified to NSF/ANSI 455-2 standards. Validates adherence to 21 CFR 111 Good Manufacturing Practices.

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FDA registered facility record
Regulatory Context

FDA Registered Facility

Official facility registration record maintained in accordance with applicable U.S. food facility registration requirements.

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ISO 22000 food safety certification mark
Food Safety

ISO 22000 (HK Facility)

SGS-certified Food Safety Management System supporting process control and hazard management.

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ISO 14644 cleanroom certification record
Cleanroom

ISO 14644 Cleanroom

Class 7 cleanroom certification confirming compliance with air purity and particle control requirements.

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HACCP certification mark
Safety System

HACCP Certified

Preventive safety management approach designed to identify, evaluate, and control relevant hazards.

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ISO 22000 USA facility certification mark
Food Safety

ISO 22000 (USA Facility)

Certified management system supporting the relevant production scope for dietary supplement operations.

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Halal certification mark
Market Access

Halal Certification

Supports compliance with applicable halal production requirements for relevant markets.

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Good Hygiene Practices certification mark
Hygiene

GHPs Certification

Good Hygiene Practices documentation supporting sanitation and hygiene controls throughout production.

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Certificate of Analysis document
Quality Control

Certificate of Analysis (COA)

Batch-level testing documentation summarizing product specifications and quality indicators.

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Manufacturing Standards

A documented framework for product quality review.

AIDEVI products are manufactured under quality-controlled processes designed to support documentation, consistency, and product quality review.

For dietary supplements, current good manufacturing practice (cGMP) requirements are intended to help ensure that products are manufactured, packaged, labeled, and held under appropriate controls. These controls help support product identity, composition, and quality review.

AIDEVI Manufacturing Standards Framework

01
Raw material qualification procedures
02
Controlled manufacturing and packaging processes
03
Documentation and recordkeeping practices
04
Batch-level review and quality records

We use this framework to support a more transparent approach to product quality communication.

Step 01

Raw Material Qualification

Selected incoming materials may be reviewed against internal quality specifications before production.

Step 02

Manufacturing Controls

Production, packaging, and labeling operations follow documented quality procedures.

Step 03

Documentation & Review

Quality records help support traceability, review, and consistency across selected batches.

Step 04

Batch Records

Batch-related documentation may be connected to specific reports or support records.

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Third-party testing and quality documentation review
Third-Party Testing Overview

Testing scope should be clear before the claim is made.

Selected AIDEVI products may be reviewed through third-party testing or independent quality documentation, depending on the product and batch. Our commitment to transparency is intended to help customers understand the available safety and quality records.

Testing scope may help support review of
  • Identity: Confirmation of ingredient profiles.
  • Purity: Absence of unwanted additives.
  • Composition or strength: Potency alignment.
  • Contaminant screening: Heavy metals and microbial safety.

Testing scope may vary by product, ingredient profile, and batch documentation status. Where records are available for public review, they will be linked below or accessible through lot-based lookup.

01

Identity Review

Helps support confirmation that the tested material matches the intended ingredient profile.

02

Purity & Composition

May include selected information related to purity, composition, or specification alignment.

03

Batch Records

Some records may be tied to specific lot numbers, product runs, or dated reports.

COA Reading Guide

How to Read a Certificate of Analysis (COA)

A Certificate of Analysis (COA) is a batch-specific document that summarizes selected quality test results for a product or ingredient. Depending on the testing scope, a COA may include information related to identity, purity, composition, specification ranges, and report dates.

What to Look For
01

Product Name or SKU

Confirms which product or ingredient the document refers to.

02

Lot Number

Shows the batch identifier linked to the tested material or finished product.

03

Report Date

Indicates when the testing or documentation was completed.

04

Test Items

Lists the specific parameters reviewed in the report.

05

Result / Specification

Shows the reported outcome and applicable specification used for comparison.

If you are unsure how to read a COA, you can search by lot number below or contact our support team for guidance.

FAQ

Frequently Asked Questions

Find clear answers before you review a record. Documentation availability may vary by product, batch, and report status.

What is a COA?

A COA, or Certificate of Analysis, is a batch-specific document that may summarize selected quality test results for a product or ingredient.

Does FDA approve dietary supplements?

Dietary supplements are not approved by FDA in the same way as prescription drugs. Manufacturers are responsible for ensuring their products are safe and properly labeled.

What does cGMP mean?

cGMP refers to current good manufacturing practice requirements that apply to manufacturing, packaging, labeling, and holding operations for dietary supplements.

Are all reports public?

Not always. Public documentation availability may vary by product, batch, and documentation status.

How do I find my lot number?

Your lot number is typically printed on the bottle, label, cap area, or outer package.

What if my lot number is missing?

Please contact support and share your product name, purchase source, and any package photos if available.

How can I request more documentation?

If you have a product-quality question, please contact our support team and we will review available information.

Need Help Reviewing a Record?

A quality question is worth documenting.

If you have a question about a lot number, a product-quality record, or a report listed on this page, please contact our support team.

Please include your product name, lot number, and purchase source so our team can assist you more efficiently.

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Important Notice

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.