Sanmina recently announced that it has received FDA registration at its Chennai, India manufacturing facilities.
The registration allows for the company to manufacture finished medical instruments and devices in India.
Sanmina is the first tier 1 electronic manufacturing services company to have FDA registration in India. The FDA registration ensures that manufacturing controls and documentation are available during the production of finished medical products to guaranteed the safety, quality and regulatory control of those products.
“For nearly a decade, Sanmina’s Chennai facility has been collaborating with customers to produce innovative medical products,” said Charlie Mason, senior VP of the medical market segment at Sanmina, in a press release. “Our medical customers can now leverage our extensive capabilities in India to design and deliver finished medical products.”
The FDA registration also allows the company to make finished products like imaging systems, blood glucose meters, patient monitors and other complex medical instruments and devices.
“Sanmina has been at the forefront of product design and manufacturing in India, establishing a proven track record across many industries in one of the fastest growing economies in the world,” said Michael Landy, executive VP and chief operating officer of Integrated Manufacturing Solutions (EMS), Asia and Europe at Sanmina. “The new FDA registration reflects our continued commitment to provide the most comprehensive range of services to OEM customers around the world.”