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Inventory Ready
Editorial status
Listed · source-checked
Last reviewed
Apr 19, 2026
Next review due
Apr 11, 2027
Commercial relationship
Listed editorially
Challenge window
Self-reported certifications labeled

CONTRACT MANUFACTURING

F.A.M.E. Health Labs

F.A.M.E. Health Labs LLC is an FDA-registered dietary supplement contract manufacturer in Cedartown, Georgia. The facility produces capsules, tablets, powders, gummies, softgels, and liquids, with packaging and fulfillment services on site. FDA Registration #18195575660.

Cedartown, Georgia

Directory Listing · Records Reviewed

Public records and independent sources have been reviewed.

What this means →
MOQ
Flexible; Pilot Program requires 30,000+ units
LEAD TIME
8-10 weeks standard; 4 weeks on Pilot Program (30,000+ units)
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§1Editorial assessment

F.A.M.E. Health Labs LLC is an FDA-registered dietary supplement contract manufacturer in Cedartown, Georgia. The facility produces capsules, tablets, powders, gummies, softgels, and liquids, with packaging and fulfillment services on site. FDA Registration #18195575660.

cGMP (Current Good Manufacturing Practice)FDA Facility RegistrationNSF InternationalPrivate LabelFormulationDosage FormSupplement Packaging

§2Our review

The six checks in our review, applied before any name appears in the directory. Each check is auto-derived from public evidence on this profile.

Independent confirmation: warn.
Sources we traced: pass.
How recent: pass.
Right to respond: pass.
What they told us: pass.
What we don’t know: miss.

§3Inspection history

§4Certifications

0 of 8 certifications independently confirmed. What this means

cGMP Compliant(Self-Reported)FDA Registered(Self-Reported)NSF Certified(Self-Reported)SQF Certified(Self-Reported)USDA Organic(Self-Reported)Non-GMO Project Verified(Self-Reported)Kosher(Self-Reported)Halal(Self-Reported)

§5Capability matrix

PRODUCT TYPES
Capsules · Tablets · Powders · Gummies · Softgels · Liquids
CAPABILITIES
Private Label · Custom Formulation · Packaging · Order Fulfillment
DOSAGE FORMS
capsules · tablets · powders · gummies · softgels · liquids

§6Sources

Dietary supplement manufacturers must comply with 21 CFR Part 111 (Current Good Manufacturing Practice for dietary supplements). This includes requirements for personnel, facilities, equipment, production, laboratory operations, and record-keeping.

Disclosures

  • No material connection exists between Inventory Ready and this manufacturer

For the check-by-check breakdown that produces this vendor's score, see our scoring framework. The connection map between F.A.M.E. Health Labs and other vendors, capabilities, and certifications is in the manufacturer atlas.

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Educational information only. Not legal, regulatory, or professional advice. Inventory Ready provides independent assessments based on publicly available information. See Terms for details.