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Latham Industries Attains ISO 13485:2016 Certification for Medical Devices
November 7, 2023 | Latham IndustriesEstimated reading time: 1 minute
Latham Industries, a renowned electronics contract manufacturer headquartered in Phoenix, proudly announces its achievement of the ISO 13485:2016 certification for medical devices. This significant milestone reflects the company's commitment to delivering quality, safety, and reliability in the design, development, and production of electronic components and assemblies for the medical industry.
The ISO 13485:2016 standard is a globally recognized quality management system that outlines the requirements for a comprehensive quality system dedicated to medical devices. This standard encompasses critical aspects such as risk management, regulatory compliance, customer satisfaction, and continuous improvement. With the attainment of this certification, Latham Industries has demonstrated its capability to meet the highest standards of quality and performance within the medical device sector.
Latham Industries is a trusted provider of electronics contract manufacturing services, catering to clients across various industries, including aerospace, medical, automotive, and industrial sectors. The company specializes in printed circuit board assembly, offering services that encompass prototyping, cable and wire harness assembly, box build assembly, and rework and repair. With the ISO 13485:2016 certification, Latham Industries has expanded its service offerings to the medical device industry, one of the fastest-growing and most demanding markets globally.
Tracey Latham, the Founder and CEO of Latham Industries, expressed, "We take immense pride in achieving the ISO 13485:2016 certification, which underscores our dedication to quality and excellence. We are thrilled to broaden our capabilities and serve the medical device industry, a strategic growth area for our company. We eagerly anticipate collaborating with our existing and new customers to provide innovative and reliable solutions for their medical device requirements."
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