Lab Reports & Manufacturing Standards
Learn how AIDEVI documents manufacturing standards, third-party testing, and batch-level quality records for selected products.
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
Official facility registration record maintained in accordance with applicable U.S. food facility registration requirements.
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ISO 22000 (HK Facility)
SGS-certified Food Safety Management System supporting process control and hazard management.
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ISO 14644 Cleanroom
Class 7 cleanroom certification confirming compliance with air purity and particle control requirements.
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HACCP Certified
Preventive safety management approach designed to identify, evaluate, and control relevant hazards.
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ISO 22000 (USA Facility)
Certified management system supporting the relevant production scope for dietary supplement operations.
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Halal Certification
Supports compliance with applicable halal production requirements for relevant markets.
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GHPs Certification
Good Hygiene Practices documentation supporting sanitation and hygiene controls throughout production.
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Certificate of Analysis (COA)
Batch-level testing documentation summarizing product specifications and quality indicators.
View Report →Manufacturing Standards
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:
- ✔ Raw material qualification procedures
- ✔ Controlled manufacturing and packaging processes
- ✔ Documentation and recordkeeping practices
- ✔ Batch-level review and quality records
We use this framework to support a more transparent approach to product quality communication.
Raw Material Qualification
Selected incoming materials may be reviewed against internal quality specifications before production.
Manufacturing Controls
Production, packaging, and labeling operations follow documented quality procedures.
Documentation & Review
Quality records help support traceability, review, and consistency across selected batches.
Batch Records
Batch-related documentation may be connected to specific reports or support records.
Third-Party Testing Overview
Selected AIDEVI products may be reviewed through third-party testing or independent quality documentation, depending on the product and batch. Our commitment to transparency ensures that your supplements meet rigorous safety benchmarks.
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.
Identity Review
Helps support confirmation that the tested material matches the intended ingredient profile.
Purity & Composition
May include selected information related to purity, composition, or specification alignment.
Batch Records
Some records may be tied to specific lot numbers, product runs, or dated reports.
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
Product Name or SKU
Confirms which product or ingredient the document refers to.
Lot Number
Shows the batch identifier linked to the tested material or finished product.
Report Date
Indicates when the testing or documentation was completed.
Test Items
Lists the specific parameters reviewed in the report.
Result / Specification
Shows the reported outcome and the 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.
| Contact Our Team |
Frequently Asked Questions
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.
Missing lot number?
Please contact support and share your product name, purchase source, and any package photos if available.
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?
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.
| Contact Support |
Please include your product name, lot number, and purchase source so our team can assist you more efficiently.
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