Genvid Lab Inc
Maker of capsules, tablets and powders with independent production rooms in its own facility.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
Genvid Lab is a dietary supplement contract manufacturer operating its own facility and headquarters at 509 NE 189th Street in Miami, Florida (founded 2020), with six independent production rooms and a stated capacity of approximately 60,000 bottles per day across capsules, tablets, and powders. The facility is listed in the NSF public directory as certified to the NSF/ANSI 455-2 dietary supplement Good Manufacturing Practice standard, with dry formulation, encapsulation, mixing, and tablet compression among its listed product technologies. Genvid Lab also reports Kosher and GMP certification. Minimum order quantities and lead times are not publicly posted.
Certifications
1 of 3 certifications independently confirmed. What this means
Capabilities
- PRODUCT TYPES
- Capsules · Tablets · Powders
- CAPABILITIES
- Custom formulas · Private label or white label · Packaging
- DOSAGE FORMS
- capsules · tablets · powders
Sources
- Genvid Lab - Official Website(2026-06-24)
- NSF/ANSI 455-2 GMP Directory(2026-06-24)
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- The company website also lists liquid and cream forms; the NSF/ANSI 455-2 listing confirms dry formulation, encapsulation, and tablet compression (capsule, tablet, and powder scope), so liquid and cream forms are website-claimed and not separately confirmed
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between Genvid Lab Inc and other vendors, capabilities, and certifications is in the manufacturer atlas.
Enforcement screening: included in Inventory Ready's most recent completed pass against FDA's published recall datasets (2026-07-09). Method and limits →
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