Factory & Quality

Red Kangaroo International

Red Kangaroo International Biotechnology (Guangzhou) Co., Ltd. provides the factory reference for RUGG. Supplied materials describe formulation, sampling, production and quality-control services.

Documented production scope

The supplied food production licence lists beverages, convenience foods and confectionery. Product-specific manufacturing scope and market requirements must be confirmed before ordering.

FACTORY & QUALITY

Certificate information

Supplied certificate copies are available for review. Current validity, scope and product coverage are confirmed for each project.

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Food Production License

Guangzhou food production authority

Documented licence · scope to be reviewed

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FSSC 22000

NSF Certification, LLC

Food safety management system · supplied copy

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HACCP

NSF Certification, LLC

Hazard analysis and critical control points · supplied copy

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Indonesia Halal Certificate

BPJPH / Republic of Indonesia

Health supplement category · product appendix applies

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FDA Facility Registration

Third-party FDA registration verification

Facility registration · not product approval

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HCS Halal Certificate

Halal Certification Services Chongqing

Attached product scope applies · supplied copy

Additional certificates & scope documents ＋

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Business License

Chinese business registration authority

Legal entity document · supplied copy

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Food Production Scope

Food production licence appendix

Production categories and scope · supplied copy

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FDA Facility Product Categories

FDA registration verification appendix

Registered facility categories · not product approval

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BRCGS Food Safety

NSF Certification, LLC

Food safety standard · current validity to confirm

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NSF GMP Dietary Supplements

NSF International

Dietary supplement GMP · current validity to confirm

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Indonesia Halal Decree

Majelis Ulama Indonesia

Halal decree · attached product list applies

Document dates and scope are transcribed from supplied copies. Some copies show dates that require renewal confirmation. The FDA document is a facility registration record, not FDA product approval.