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ISO 9001:2015

This certification is a quality management standard that represents our commitment to business efficiency and customer satisfaction.


Through Latham Industries’ quality management system (QMS), we increase productivity, reduce unnecessary costs, and ensure the highest quality of processes and products.


ISO 13485:2016

This certification is an international standard that defines criteria for a QMS for medical device manufacturing.

Latham Industries is now certified to manufacture medical devices and provide related services that consistently meet customer and applicable regulatory requirements. 


21 CFR 820

This compliance is a set of regulations from the FDA that outlines the good manufacturing practice (GMP) requirements for manufacturers of finished medical devices.


Latham Industries is 21 CFR 820 Compliant and meets the requirements for GMP.  This is another step Latham has taken to ensure medical devices are safe and built to the highest standards.



This certification trains Latham Industries' staff to IPC Acceptability of Electronic Assemblies standards. We maintain continuous certification to the current IPC workmanship skills/inspection modules, ensuring our staff delivers top quality in all our assembly work.



Quality certification to ensure Latham Industries’ staff is able to protect sensitive components from electrostatic discharge (ESD) at every step of assembly.

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