AVIVA Natural Supplements: due-diligence report
Public-record summary and buyer worksheet. Records can be incomplete; a listing is not product approval, an audit result or a guarantee of suitability. This report updates as source records change. Print a dated copy to retain the version you reviewed.
Share this report: https://certifiedmanufacturers.com/manufacturers/aviva-natural-supplements/due-diligence
Profile last verified: Oct 12, 2026. Report printed / reviewed on: ____________________
Certifications and licences
NPA GMP certified
Issuer: Natural Products Association. Registry status: active. Checked: Oct 12, 2026.
Reference: i24-1100096-1, a24-1100096-1. Expiry: Feb 15, 2028.
Scope: Manufacturing and packaging of dietary supplement capsules, tablets and powders; packaging of dietary supplement softgels
Registry source: https://www.npanational.org/certifications/npa-gmp-certification-program/gmp-certified-companies/Facilities
AVIVA Natural Supplements, 26 Van Dyke Ave, New Brunswick, NJ, 08901, US — manufacturing; source: NPA GMP; checked Oct 12, 2026.
AVIVA Natural Supplements, 7A Jules Lane, New Brunswick, NJ, 08901, US — packaging; source: NPA GMP; checked Oct 12, 2026.
AVIVA Natural Supplements, 24 Van Dyke Avenue, New Brunswick, NJ, 08901, US — distribution; source: NPA GMP; checked Oct 12, 2026.
FDA inspection history
Dataset date: Oct 22, 2026. Facility records are matched by company and location; confirm that the site is the one in your quote. FDA inspection source.
May 19, 2026 — NAI: No action indicated
Aviva Natural Supplements, LLC, New Brunswick, New Jersey, United States. FEI: 3022297128; inspection: 1318276.
Food Composition, Standards, Labeling and Econ
Feb 27, 2026 — OAI: Official action indicated
Aviva Natural Supplements, LLC, New Brunswick, New Jersey, United States. FEI: 3022297128; inspection: 1272461.
Food Composition, Standards, Labeling and Econ, Foodborne Biological Hazards
21 CFR 111.10(b): Hygienic practices
21 CFR 111.20(d): Physical plant - design
21 CFR 111.70(b): Specifications - components
21 CFR 111.70(e): Specifications - finished dietary supplement
21 CFR 111.75(a)(2)(ii)(A): Component - qualify supplier
21 CFR 111.75(a)(2)(ii)(B): Component - certificate of analysis
21 CFR 111.75(c): Specifications met - verify; finished batch
21 CFR 111.110: Quality control - Laboratory control processes; production, process control
21 CFR 111.113(a)(1): Quality control production, process control; material review, disposition
21 CFR 111.210: Master manufacturing record - record requirements
21 CFR 111.260: Batch record - required information
21 CFR 111.315(d): Standard reference materials; criteria for selecting
21 CFR 111.320(b): Examination, testing; scientifically valid
Apr 14, 2022 — NAI: No action indicated
Aviva Natural Supplements, LLC, New Brunswick, New Jersey, United States. FEI: 3022297128; inspection: 1168552.
Food Composition, Standards, Labeling and Econ
Apr 14, 2022 — NAI: No action indicated
Aviva Natural Supplements, LLC, New Brunswick, New Jersey, United States. FEI: 3022297128; inspection: 1168614.
Food Composition, Standards, Labeling and Econ
FDA recalls
Dataset date: Oct 27, 2026. Recall matches use company names and may concern a different product or facility.
No matched recall events in the imported dataset. This is not proof of a recall-free history.
Company website claims — not registry verified
Last website check: Oct 16, 2026.
“Some of the products we can blend, but are not limited to, include superfood green formulas, protein formulas, pre and post workout powders, other herbal powders, collagen powders, and beverage blends.”
Last seen Oct 16, 2026. https://avivanaturals.com/capabilities/
“Aviva Natural Supplements is a trusted contract manufacturer of nutraceuticals, dietary supplements and vitamins.”
Last seen Oct 16, 2026. https://www.avivanaturals.com
“Aviva Natural Supplements is a full-service contract manufacturer offering high quality products at fair prices.”
Last seen Oct 16, 2026. https://avivanaturals.com/capabilities/
“We offer turnkey solutions - from ingredient sourcing to in house custom packaging”
Last seen Oct 16, 2026. https://avivanaturals.com/capabilities/
“We work with customers for all their custom packaging requirements, including label design.”
Last seen Oct 16, 2026. https://avivanaturals.com/capabilities/
“Aviva is HALAL Certified manufacturing company.”
Last seen Oct 16, 2026. https://avivanaturals.com/facilities/
“We offer a range of USDA Certified Organic supplements to our customers.”
Last seen Oct 16, 2026. https://avivanaturals.com/facilities/
“We work with brands across the globe, including USA, UK, Europe, Canada.”
Last seen Oct 16, 2026. https://www.avivanaturals.com
Evidence to request from the manufacturer
Public records cannot answer these questions. Mark each item after reviewing the evidence. Blank means not assessed, not a failed audit. Notes entered here are not saved or included in a shared URL.
Request role-specific training records and the named quality contact.
21 CFR 111.12Request a site walkthrough, sanitation controls and equipment maintenance records (also §111.25).
21 CFR 111.20Request written identity, purity, strength, composition and contaminant specifications for your product.
21 CFR 111.70Ask how each dietary ingredient is identified and how suppliers and certificates of analysis are qualified.
21 CFR 111.75Request quality control procedures, release authority and handling of deviations and rejected batches.
21 CFR 111.105Request the approved product-specific master manufacturing record and change-control process.
21 CFR 111.205Review a completed batch record with traceability to components, processing and release.
21 CFR 111.255Request scientifically valid test methods, sampling plans and laboratory controls for your specifications.
21 CFR 111.315Request procedures that prevent label mix-ups and control packaging and label reconciliation.
21 CFR 111.403Ask how storage conditions protect identity, purity, strength and composition during holding and distribution.
21 CFR 111.453Request complaint review and investigation procedures; discuss returned-product controls under §111.503.
21 CFR 111.553Confirm retention and access to records supporting your batches.
21 CFR 111.605