Electronic Assembly You Can Depend On

Certification 1.

ISO 9001:2008

All requirements of ISO 9001:2008 are generic and are intended to be applicable to all organizations, regardless of type, size and product provided.

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CERTIFICATION 2.

ISO 13485:2003

The primary objective of ISO 13485:2003 is to facilitate harmonized medical device regulatory requirements for quality management systems.

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CERTIFICATION 3.

SERIAL NO. 610-T 38004326

This certification demonstrates commitment to customer requirements and greatly assists any company dedicated to ISO-9000 or other quality assurance initiatives.

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A Full-Service Electronics Assembly Manufacturing Company

CERTIFICATE OF REGISTATION – 0093185
ISO 9001:2008 specifies requirements for a quality management system where an organization

  • Needs to demonstrate its ability to consistently provide product that meets customer and applicable statutory and regulatory requirements, and
  • Aims to enhance customer satisfaction through the effective application of the system, including processes for continual improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements.
All requirements of ISO 9001:2008 are generic and are intended to be applicable to all organizations, regardless of type, size and product provided.

CERTIFICATE OF REGISTATION – 0090574
ISO 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services.

The primary objective of ISO 13485:2003 is to facilitate harmonized medical device regulatory requirements for quality management systems. As a result, it includes some particular requirements for medical devices and excludes some of the requirements of ISO 9001 that are not appropriate as regulatory requirements. Because of these exclusions, organizations whose quality management systems conform to this International Standard cannot claim conformity to ISO 9001 unless their quality management systems conform to all the requirements of ISO 9001.

All requirements of ISO 13485:2003 are specific to organizations providing medical devices, regardless of the type or size of the organization.

If regulatory requirements permit exclusions of design and development controls, this can be used as a justification for their exclusion from the quality management system. These regulations can provide alternative arrangements that are to be addressed in the quality management system. It is the responsibility of the organization to ensure that claims of conformity with ISO 13485:2003 reflect exclusion of design and development controls.

SERIAL NO. 610-T 38004326
IPC-A-610, Acceptability of Electronic Assemblies is the most widely used standard published by the IPC. With multiple language versions, it has an international reputation as the source for end product acceptance criteria for consumer and high reliability printed wiring assemblies.

An industry developed and approved program that includes training, certification and instructional materials based on the IPC-A-610. This certification demonstrates commitment to customer requirements and greatly assists any company dedicated to ISO-9000 or other quality assurance initiatives.

This training and certification has immediate recognition, legitimacy and value throughout the electronics industry.

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Whatever it takes...surface mount, auto feed, hand solder, OSDA will just do it. They are right on the money with their builds.

- Project Manager, Fortune 50 Global Manufacturing Company