Action Pak Inc
Contract manufacturer offering powder formulation, liquid and powder filling and stick pack manufacturing.
- MOQ
- Not publicly disclosed
- LEAD TIME
- Not publicly disclosed
Overview
Action Pak Inc is a contract manufacturer and packager founded in 1979, headquartered in Camden, New Jersey, with a second facility in Bristol, Pennsylvania. The company operates a 200,000 square foot food production facility plus an additional 35,000 square feet for non-food products. Action Pak provides powder formulation services for dietary supplements alongside liquid and powder filling, stick pack manufacturing, kitting, labeling, and packaging-design services. The company holds SQF certification (registry-confirmed 2026-07-05 at its Camden, New Jersey food facility) and self-reports FDA registration, USDA registration, Kosher certification, Pennsylvania Certified Organic (PCO) certification, and ISTA testing certification. Reported clients include Heinz and Johnson and Johnson, suggesting infrastructure suited for established consumer brands. Annual revenue is reported in the 10 to 50 million dollar range with 51 to 250 employees per third-party business directories. Form-factor focus is powder and liquid based, with capability to format products into bottles, single-serve sticks, and pouches.
Certifications
1 of 4 certifications independently confirmed. What this means
Capabilities
- PRODUCT TYPES
- Powders · Liquids · Stick Packs
- CAPABILITIES
- Custom formulas · Packaging · Label or package design
- DOSAGE FORMS
- powders · liquids · stick-packs
Sources
- SQFI SQF Certified Site Directory — registry confirmation (independent)(2026-07-05)
- Action Pak Inc - Official Website(2026-05-25)
- Action Pak - Powder Formulation Services(2026-05-25)
- Action Pak - SQF Facilities(2026-05-25)
What we couldn't verify
We did not visit this company on site. See the limits that apply to every listing.
- Share of capacity dedicated to dietary supplements across the Camden NJ food facility and the Bristol PA non-food operations
- Share of revenue from dietary supplements vs food, beverage, and consumer packaged goods
- FDA inspection classification history
- ISTA certification scope
- All claimed certifications are self-reported; no independent directory verification completed during this source-checked assessment
- Form-factor scope is powder and liquid focused; does not manufacture tablets, capsules in-house, softgels, or gummies as standalone contract-manufacturing services
- Significant share of stated capability is packaging and kitting rather than primary supplement formulation; buyers should clarify scope expectations during RFQ
Dietary supplement manufacturers must comply with 21 CFR Part 111 (cGMP). What Part 111 requires
The connection map between Action Pak 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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