River Bend Times

Titronics Research & Development Co. in Tiffin, Iowa was inspected by the Food and Drug Administration (FDA) on July 9 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:

'Document control procedures have not been adequately established.'

'Calibration procedures do not include specific directions and limits for accuracy and precision and provisions for remedial action.'

'Procedures have not been adequately established to control product that does not conform to specified requirements.'

'Procedures for device history records have not been adequately established.'

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.