Tuesday, May 22, 2018
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Saline Lectronics Conforms to FDA PCB Standards
Saline, MI — Saline Lectronics, Inc.'s Saline, MI facility is now cGMP compliant and registered by the Food and Drug Administration (FDA). These certifications, along with the company's current ISO 13485 standard, demonstrate the company's ongoing dedication to providing high-quality circuit board assemblies for medical applications.

As a full service EMS provider serving the medical market, Saline Lectronics has many customers that require strict quality codes that follow FDA-Good Manufacturing Practice (cGMP) standards defined by the FDA 21 CFR (Code of Federal Regulations) Part 820 QSR (Quality System Regulation). To qualify for this QSR, the company demonstrated its ability to implement a quality system for designing, manufacturing, packaging, labeling, stocking and delivering medical devices sold within the United States.

The company serves low- to mid-volume manufacturers in a wide variety of medical fields including biomedical, cardiovascular, wound care, lasik technology and portable imaging equipment, to name a few. Some of its services include contract design supporting DFX for manufacturing, assembly of manufacturing technologies, circuit board testing, and final product assembly to the pack-out level (box builds).

Saline Lectronics provides the latest manufacturing expertise including THT, SMT, BGA, microBGA and different bottom terminated component capabilities, as well as other challenging mixed-technology assemblies.

Contact: Saline Lectronics, Inc., 710 North Maple Road, Saline, MI 48176 734-944-2120 fax: 734-944-2005 E-mail: msciberras@lectronics.net Web:

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