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FDA Inspection Passed with Flying Colours

FDA inspection passed with flying colours

FDA Inspection Passed with Flying Colours

Europlaz Technologies Limited, a medical device manufacturer, is delighted to announce that it has passed its latest US Food and Drug Administration (FDA) inspection with flying colours.

Following an inspection of our premises in Southminster, Essex, Europlaz, as a finished medical device moulding and assembly specialist was found to be fully compliant with Good Manufacturing Practice (GMP) – meaning our products are manufactured to the highest possible quality.

The US Food and Drug Administration (FDA)

Regulatory agencies like the U.S. Food and Drug Administration (FDA) used to focus primarily on domestic GMP compliance and enforcement. But the number of FDA inspections abroad has grown as importers increasingly source products abroad.

FDA inspection

From the FDA website:

The Food and Drug Administration (FDA) conducts inspections and assessments of regulated facilities to determine a firm’s compliance with applicable laws and regulations, such as the Food, Drug, and Cosmetic Act and related Acts.

FDA inspects manufacturers or processors of FDA-regulated products to verify that they comply with relevant regulations.

Those inspected include:

vaccine and drug manufacturers

blood banks

food processing facilities

dairy farms

animal feed processors

compounding pharmacies

FDA also inspects:

facilities that conduct studies in people (clinical trials)

laboratories that conduct studies in animals or microorganisms when these studies are used to apply for FDA approval of a medical product

foreign manufacturing and processing sites for FDA-regulated products that are sold in the United States

imported regulated products at the border

FDA conducts several types of inspections to help protect consumers from unsafe products:

pre-approval inspection after a company submits an application to FDA to market a new product

routine inspection of a regulated facility

“for-cause” inspection to investigate a specific problem that has come to FDA’s attention

Well done to the whole team at Europlaz for all their continued hard work and commitment to their roles. This achievement would not have been possible without a team effort.

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