Kamwo Meridian Herbs dispensary is registered with the FDA and open to regular inspections from their agents to confirm cGMP compliance. We are proud to be the only herbal dispensary to open their doors to the FDA in an effort to maintain higher standards of quality control, as well as acting as a liaison for the profession.

We employ NCCAOM certified herbalists and a Western Pharmacist to oversee the processing of your order. Raw and vacuum pack formulas go through a 6 point safety check. Granule and capsule orders are filled through our Herbal Dispensary Management System (HDMS) automated system, to ensure you always receive the right product at the right dose.

As an FDA-registered facility, Kamwo is subject to regular inspections and audits by the FDA.  In order to comply with cGMP regulations, Kamwo’s Granule Dispensary relies on the HDMS system to achieve these standards.

HDMS ensures FDA cGMP requirements are met through computer integration with a barcode scanner and an electronic scale.

Is your Granule Dispensary Compliant with FDA cGMP regulations?

As part of cGMP compliance, each dispensary must have a system/method to prevent contamination, mix-ups, deviations, failures, and errors. To pass the inspection, FDA verifies Granule Compounding Operating procedures complies with prevention of contamination, mix-ups, deviations, failures, and errors.

Is your Granule Dispensary considered 'adulterated' by FDA?

Here is the 'adulterated' definition from FDA's website: 'If a company is not complying with CGMP regulations, any drug it makes is considered “adulterated” under the law. This kind of adulteration means that the drug was not manufactured under conditions that comply with CGMP. It does not mean that there is necessarily something wrong with the drug.'