Muncie Reporter

First Call, Inc. in Winona Lake, Indiana was inspected by the Food and Drug Administration (FDA) on July 19 for post-market assurance for devices and received four citations, according to data posted on the FDA’s official website.

The FDA website indicates that the citations were delivered to the company as follows:

'Individuals who conduct quality audits have direct responsibility for the matters being audited.'

'The design history file was not established.'

'Procedures to ensure that all purchased or otherwise received product and services conform to specified requirements have not been adequately established.'

'The device history record does not include, or refer to the location of any unique device identifier (UDI) or universal product code (UPC).'

The FDA routinely inspects facilities across the nation to determine if the workplaces and their products are compliant with FDA-regulated laws and regulations implemented to improve overall public health. Inspection results are then disclosed publicly for businesses to consistently make smarter business decisions for the future.

The FDA is a government agency that is primarily responsible for monitoring the manufacturing and distribution of human and animal drugs, biological products, medical supplies and tobacco products for safety quality, according to its website.