Bedfont® Scientific Limited, a medical device manufacturer, has passed its latest US Food and Drug Administration (FDA) inspection with flying colours.
Following an inspection of its premises in Kent, UK, the breath analysis specialist was found to be fully compliant with Good Manufacturing Practice (GMP) – meaning its products are manufactured to the highest possible quality.
Louise Bateman, QA & RA Manager, stated, “With this outcome, it shows we are working as a compliant company to FDA standards and are able to continue to provide high-quality products to the US.”
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