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Manufacturing facility · Cedartown, Georgia

Where your supplement is manufactured.

Ingredients, formulation, manufacturing, testing and packaging run on our campus in Cedartown, Georgia, with one team accountable from raw material to released batch.

  • 152+ acre campus
  • Five formats manufactured in-house
  • curí ISO/IEC 17025 lab on campus
  • FDA-registered · cGMP · NSF GMP · SQF
Operator charging a blender on the F.A.M.E. production floor
Capacity

What our lines produce, each day.

100M+
capsules a day
Encapsulation
100K+
bottles a day
Bottling
40K+
powder bottles a day
Powder filling
50K+
sachets and stick packs a day
Flexible packs

Plus 400M+ stick packs a year on purpose-built lines. Four weeks on repeat and stock runs of 30,000+ units, from production start. Planned: capacity doubling by Q4 2026.

How a run moves

From raw material to released batch, without a hand-off.

  1. 01

    Ingredients

    F.A.M.E. Ingredients holds 10,000+ raw actives on site. Each lot's identity is confirmed on arrival.

  2. 02

    Formulation

    In-house R&D and our Flavor Lab, with 1,000+ flavors in active rotation.

  3. 03

    Manufacturing

    Blending, encapsulation, tablet compression, powder filling, gummies and liquids, all on our own lines.

  4. 04

    Testing

    Every batch is tested in-house before release, and our certificate of analysis ships with every batch. curí, the third-party ISO/IEC 17025 accredited lab on our campus, can run further tests or issue an accredited COA on request, at an additional fee, with no handover delays.

  5. 05

    Packaging

    Bottling, labeling and kitting in house, into bottles, jars, stick packs and pouches.

Softgels are manufactured by a qualified partner and tested in-house before release.

Inside the facility

The floor where your product runs.

Formats

Five formats on our own lines.

Softgels are also available, manufactured by a qualified partner and tested in-house. Softgels →

Equipment

A sample of the machines on the floor.

Ratings are the manufacturers' figures. This is a selection, not the full line list.

  • NJP-7500 automatic capsule fillerRated by the manufacturer at up to 7,500 capsules a minute.
  • KLS-225 capsule fillerRated by the manufacturer at up to 225,000 capsules an hour.
  • KLS-75 capsule fillerRated by the manufacturer at up to 75,000 capsules an hour, with fast changeover.
  • NJP-2000 automatic capsule fillerAutomatic filling from feeding to output, GMP compliant.
  • NP-255 tablet pressRated by the manufacturer at up to 192,000 tablets an hour, with Natoli AIM ProPlus controls.
  • Countec DMC 60T tablet counterRated by the manufacturer at up to 6,000 tablets a minute, with infrared count verification.
  • E2-Entrada pouch fillerPLC-controlled pouch filling with a touch-screen interface.
Quality control

Every batch is tested before it leaves.

Three checkpoints, every run.

  1. 1

    Raw materials

    Vetted suppliers. Identity confirmed on arrival.

  2. 2

    During the run

    Blend uniformity, weight and hardness checked in process.

  3. 3

    Before release

    Potency, micro and stability confirmed in-house. Our certificate of analysis ships with every batch.

Certifications and registrations

The paperwork buyers ask for, on file.

FDA-registered facility

Registered with the FDA as a dietary supplement manufacturer (registration 18195575660).

cGMP

Manufactured to current Good Manufacturing Practice for dietary supplements, 21 CFR Part 111.

NSF GMP certified (NSF/ANSI 455-2)

NSF GMP certification demonstrates a commitment to dietary supplement quality and compliance with U.S. GMP requirements. It covers capsules, gummies, powders and tablets.

SQF certified

The SQF Code for Dietary Supplements Manufacturing, Edition 9, with HACCP-based food safety plans.

MOSA Certified Organic

Certified organic handling under the USDA National Organic Program (NOP ID 9950013473).

Health Canada Site Licence

Held since October 2024, for brands selling in Canada.

ISO/IEC 17025 (curí)

curí, the third-party testing lab on our campus, is accredited to ISO/IEC 17025:2017.

NSF GMP for Sport registration

Sports lines manufactured here can go through NSF Certified for Sport, a separate product certification.

Halal and Kosher certification can be supported for individual products. Certificates are available on request.

See all certifications, ownership and what each one covers
The campus

152+ acres in Cedartown, Georgia.

Manufacturing at 3520 Lees Chapel Road, with warehousing at 641 Tenth Street, both in Cedartown and both on our NSF certificate.

About 60 miles from Atlanta's Hartsfield-Jackson airport, with direct I-20 access. More manufacturing space is underway on the same land.

Concept render of the planned F.A.M.E. campus
Concept render of the campus with planned facilities, from the north.
Questions

About the facility.

Can I visit the facility?

Yes, by appointment, Monday to Friday, 8am to 4pm. Tell us what you're building and we'll set a time.

Which formats are manufactured on your campus?

Capsules, tablets, powders, gummies and liquids. Softgels are manufactured by a qualified partner and tested in-house before release.

Is every batch tested?

Yes. Every batch is tested in-house before release and ships with our certificate of analysis. curí, the third-party ISO/IEC 17025 accredited lab on our campus, can issue an accredited COA on request, at an additional fee.

Which certifications does the facility hold?

FDA registration, cGMP, NSF GMP certification (NSF/ANSI 455-2), SQF, MOSA Certified Organic and a Health Canada Site Licence. curí is accredited to ISO/IEC 17025.

Where is the facility?

3520 Lees Chapel Road, Cedartown, GA 30125, about 60 miles from Atlanta.

See where your product would be manufactured.

Facility visits by appointment. We reply to quote requests within 24 to 48 hours.