What is the purpose of an FDA inspection?

The primary purpose of an FDA inspection is to ensure compliance with regulations and to evaluate manufacturing processes and quality systems. Inspections are critical for verifying that manufacturers adhere to the standards set forth by the FDA, which are designed to guarantee the safety and efficacy of medical devices and other products that fall under FDA jurisdiction. During these inspections, FDA representatives assess not only the operational procedures of a facility but also how well the manufacturer adheres to the established quality systems. This comprehensive evaluation helps to identify potential issues that may affect product safety or quality, ensuring that the public is protected from substandard products.

The emphasis during inspections is not on reducing manufacturing costs, providing employee training, or focusing solely on high-cost items, but rather on the overarching goal of regulatory compliance and quality assurance across all products made by the manufacturer. Hence, the correct answer aligns perfectly with the FDA's mission to safeguard public health through rigorous oversight.