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Editorial status
Listed · source-checked
Last reviewed
Mar 12, 2026
Next review due
Mar 12, 2027
Commercial relationship
Independent listing · no commercial relationship
Challenge window
Self-reported certifications labeled

CONTRACT MANUFACTURING

Robinson Pharma

Robinson Pharma operates over 1 million sq ft of manufacturing space across eight to nine facilities in Santa Ana and Costa Mesa, California. Founded in 1989, the company has the largest softgel production capacity in the United States. Their facilities produce 23 billion softgels, 7 billion gummies, and 5 billion tablets and capsules per year. Robinson Pharma reports certifications from NSF, UL, and Eurofins, and carries ISO 9001:2015 and SQF credentials, though NSF and USP could not be confirmed through their respective public directories as of March 2026. USDA Organic certification has been independently confirmed via the USDA Organic Integrity Database. The company recently expanded with new high-speed liquid production lines and additional tablet capabilities. They serve brands that need high-volume production runs with claims of the shortest lead times in the industry. Their facility count has grown from seven to nine buildings in recent years, funded partly by a $40.7 million property acquisition.

Santa Ana, California

IRASSESSED· Enforcement Records Reviewed

FDA enforcement databases, inspection classifications, and warning letter archives reviewed. No unresolved adverse findings identified in our review.

Assessed: April 2026How we assess vendors
MOQ
Not publicly disclosed
LEAD TIME
Not publicly disclosed
Request a free introWhy we recommend this vendor · read the rationale

§1Editorial assessment

Robinson Pharma operates over 1 million sq ft of manufacturing space across eight to nine facilities in Santa Ana and Costa Mesa, California. Founded in 1989, the company has the largest softgel production capacity in the United States. Their facilities produce 23 billion softgels, 7 billion gummies, and 5 billion tablets and capsules per year. Robinson Pharma reports certifications from NSF, UL, and Eurofins, and carries ISO 9001:2015 and SQF credentials, though NSF and USP could not be confirmed through their respective public directories as of March 2026. USDA Organic certification has been independently confirmed via the USDA Organic Integrity Database. The company recently expanded with new high-speed liquid production lines and additional tablet capabilities. They serve brands that need high-volume production runs with claims of the shortest lead times in the industry. Their facility count has grown from seven to nine buildings in recent years, funded partly by a $40.7 million property acquisition.

§2Six-gate readout

Six gates we apply before any name appears in the directory. Each gate is auto-derived from public evidence on this profile.

Evidence: warn.
Provenance: miss.
Disclosure: pass.
Freshness: pass.
Challenge: pass.
Abstention: miss.

§3Inspection history

§4Certifications

2 of 8 certifications independently confirmed. What this means

§5Capability matrix

PRODUCT TYPES
Softgels · Gummies · Tablets · Capsules · Powders · Liquids
CAPABILITIES
Contract Manufacturing · Private Label · Custom Formulation · Packaging · Softgel Specialty
DOSAGE FORMS
capsules · gummies · liquids · powders · softgels · tablets

§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

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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.