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Our Facility

Located in Chatsworth, CA, Multi-Pak facilities include over 55,000 sq.ft. of manufacturing, packaging and warehouse in two adjacent buildings. The facility is designed with pharmaceutical quality in mind, with packaging equipment isolated and all processes and procedures documented in accordance with cGMP standards.​
Multi-Pak operates more than 90 different processing and packaging machines
  • Seamless floors through out to facilitate cleaning
  • microbial filtration
  • Enhanced clean rooms
  • Independent temperature controls
  • Energy efficient warehouse lighting
 
Quality Assurance
Multi-Pak’s quality control department consists of trained inspectors to ensure strict adherence to quality manufacturing standards. Our FDA Drug Manufacturing License underscores our commitment to these standards.
  • Incoming raw materials are inspected
  • 100% visual inspection of all units and final packaging
  • 100% check weighing of finished SKU’s
  • Random sampling of finished SKU’s in accordance with ANSI guidelines
  • Orders released only after QA final approval
  • Documentation that ensures conformity to customer specifications
  • Current Good Manufacturing Practice (CGMP) facilities
  • US Food and Drug Administration (FDA) registered and inspected
  • (UL Certified) Audited by UL Registrar LLC and meets cGMP requirements in conformance with FDA Regulation 21 CFR Part 111
  • (ORGANIC Certified) Audited by Organic Certifiers and meets USDA Organic Regulations 7CFR Part 205
  • (Halal Certified) Audited by IFANCA
Licenses and Permits
  • CA State FDA Drug Manufacturing
  • CA State Food Processing
  • Board of Pharmacy Drug Wholesaler​​
  • Certified to the USDA Organic Regulations 7CFR Part 205
  • Halal Certified by IFANCA
At Multi-Pak, quality is guaranteed. After all, we
have over a 60 year track record to uphold.
Improvements & Expansion
With ongoing investments in equipment, personnel and resources, Multi-Pak has substantially expanded its services, capacity and capabilities for contract packaging.

We now have additional humidity-controlled suites at our FDA-approved facility and packaging suites that can accommodate daily production volumes from thousands to millions of packs per day.

Multi-Pak can easily handle volume requirements from as little as 50,000 units up to much larger commercial runs of a 100 million plus packs in solid dose forms and powders.
 
This facility has been audited by UL Registrar LLC and meets cGMP requirements in conformance with FDA Regulation 21 CFR Part 111.
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Our Facility

More than 90 different processing and packaging machines​

Quality Assurance
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This facility has been audited by Organic Certifiers and meets USDA Organic Regulations 7CFR Part 205
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