Eevia Health’s manufacturing facility was recently inspected by the US Food and Drug Administration. The audit went very well and no obeservations were made, only informal recommendations.
Eevia Health Oy operates with a food supplement manufacturing lisence (5-2017) from Finnish food authority Ruokavirasto. In addition it is certified under ISO 22 000 and has various other certifications, including organic certificates on company and product level. The export of nutraceutical ingredients from Finland to the United States require Eevia Health Oy to be compliant with the US Good Manufacturing Practice (cGMP 21 CFR parts 110 & 111) and the FSMA (Food Safety Modernization Act).
The FDA audit confirms Eevia Health Oy quality standards and will enhance our ability to export to the US market.