Compliance

Compliance you can verify

FDA-registered Ontario production with downloadable scans. Where a published cycle has rolled, we mark it clearly and send the active renewal pack on request — not silent placeholders.

Our compliance credentials

Numbers and scans you can open — plus a clear note when a renewal pack is the current source of truth for your audit.

Production certificates are issued to the FDA-registered Ontario facility at 1500 S Milliken Ave STE B (SED Pharma Inc DBA Innova Nutra). HiGO commercial coordination uses 1927 E Francis Street, Ontario, CA — standard U.S. brand-owner / registered-facility split.

FDA Registered FacilityFDA Registered Facility
cGMP Certified FacilitycGMP Certified Facility
HACCP / GMP CertifiedHACCP / GMP Certified
California Processed Food RegistrationCalifornia Processed Food Registration
Made in USA / Certificate of OriginMade in USA / Certificate of Origin

Verify each credential

Certificate numbers, validity windows, and downloadable documents — issued to our Ontario, California manufacturing facility.

FDA Registered Facility

Current on file

U.S. Food and Drug Administration

No. 13565746238

Documented period 2025-05-05 → 2026-12-31

Ontario, California manufacturing facility Food Facility Registration — status on the published FDA search: VALID through 2026-12-31.

View certificate

cGMP Certified Facility

Current pack on request

Perry Johnson Registrars Food Safety, Inc. (PJRFSI)

No. C2025-02712

Documented period 2025-05-09 → 2026-05-08 · Active renewal documents available for buyer audits

21 CFR Part 111 / cGMP for dietary supplements — manufacturing and packaging of capsules and tablets; powder mixing and packaging into sachets and jars. Current renewal certificate pack available on request.

View last published scan

HACCP / GMP Certified

Current pack on request

Perry Johnson Registrars Food Safety, Inc. (PJRFSI)

No. C2025-02711

Documented period 2025-05-09 → 2026-05-08 · Active renewal documents available for buyer audits

HACCP/GMP as contained in 21 CFR Part 117 subpart B — Ontario facility scope covering capsules, tablets, and powder packaging. Ask sales for the active-cycle document set.

View last published scan

California Processed Food Registration

Current pack on request

California Department of Public Health, Food and Drug Branch

No. 125291

Documented period 2025-04-30 → 2026-03-28 · Active renewal documents available for buyer audits

State registration to manufacture, pack, or hold processed food in California (Registration No. 125291). Current registration confirmation available on request for audits.

View last published scan

Made in USA / Certificate of Origin

Shipment document

American World Trade Chamber of Commerce

No. AW-25-341906

Issued 2025-07-08

U.S. Certificate of Origin supporting Made-in-USA claims for export shipments from our Ontario, California production campus.

View certificate

What each certification means

FDA-Registered Facility

FDA-Registered Facility

Our Ontario manufacturing facility holds U.S. FDA Food Facility Registration No. 13565746238 (published VALID through Dec 31, 2026). Registration is the regulatory baseline for dietary supplement manufacturing in the United States.

View FDA registration proof
cGMP-Certified Processes

cGMP-Certified Processes

Independently certified by PJRFSI to 21 CFR Part 111 cGMP for dietary supplements (Certificate C2025-02712). Scope covers capsules, tablets, and powder mixing/packaging. View the published scan below; request the active renewal pack for current audits.

View cGMP certificate
HACCP / GMP Certified

HACCP / GMP Certified

PJRFSI HACCP/GMP certification under 21 CFR Part 117 subpart B (Certificate C2025-02711) documents hazard analysis and critical control across production and packaging. Current-cycle documents ship with buyer audit requests.

View HACCP certificate
Made in USA & Export Ready

Made in USA & Export Ready

Manufactured in California with Certificate of Origin and Certificate of Free Sale support for international brand partners — documentation packs available with qualifying shipments.

View Certificate of Origin

Why these certifications matter to your brand

Retailer & marketplace approval

Major retailers and platforms increasingly require FDA registration and cGMP evidence from your manufacturer before listing.

Recall protection

cGMP batch records let you scope a recall precisely to affected units — instead of pulling everything — protecting margin and reputation.

Consumer trust

Visible certifications are table-stakes trust signals. 'Manufactured in a cGMP-certified facility' is a claim consumers recognise and retailers accept on label.

Faster market entry

Documentation packs (COA, cGMP, FDA evidence, origin/free-sale where needed) ship with every batch, smoothing retail onboarding and international market entry.

Need the current audit pack?

Request FDA proof, active cGMP/HACCP cycles, California registration confirmation, COA samples, and origin/free-sale support for your buyer questionnaire.