Amherst, NY – October 8, 2009 – IIMAK Manufacturing Services, manufacturers of medical devices, industrial products, and consumer electronic supplies, announces its facility is ISO-08 (Class 100,000) clean room certified.  Furthermore, IIMAK’s facility is ISO-06 capable and compliant with ISO 14644-1 and 14644-2 for particle count testing. 

IIMAK’s ISO-08 certified clean room has the capabilities for all light assembly projects, tray and pouch sealing, hot stamp and pad printing, and sewing.  This 2,500ft² clean room environment is fully staffed by highly trained IIMAK technicians with access to state-of-the-art production equipment. 

As a niche contract manufacturer, IIMAK is small enough to quickly react and implement projects, but large enough to make significant capital investments.  “The NY-based project management team’s decision to invest in a clean room continues to competitively position IIMAK amongst other similar manufacturers”, states Dave Smith, IIMAK VP of manufacturing services.

IIMAK’s modern, temperature controlled facility is ISO 9001:2008 registered, ISO13485 registered, cGMP compliant, and ISO-08 clean room certified.  With outstanding 5+ Sigma quality systems, manufacturers will be assured of consistent high quality products that are to specification and made on time.

Located just over the border in Reynosa, Mexico, IIMAK offers shorter lead times and reduced inventory costs with quick 3 day shipments to the U.S.  IIMAK’s low cost business model, coupled with its experienced NY based project management team, can improve profitability with a customized program.  For more information about IIMAK Manufacturing Services, visit www.iimakcm.com,  or call toll-free, (877) 904-3162.

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