| Since 1987, Vistek Medical has been making news as it retools the gold standard for precision-machined parts. Browse the archives below for press releases, Vistek news and media clips about the company.
NEWS RELEASES
 MAY 14, 2009, VISTEK receives dual Certification in both ISO13485:2003 & ISO9001:2008.
Vistek is now a FDA-registered and ISO13485:2003 and ISO9001:2008 Certified medical device manufacturer. The company attributes this achievement to the staff's tremendous amount of time, effort and resources devoted to the process. During our economy's turbulent times, Vistek Medical felt strongly that it needed to invest more capital in themselves strengthening internal processes and procedures to become a world class medical device manufacturing company.
For more information on how Vistek may help your company with its medical device manufacturing needs, contact Vince Visco at 215.357.6956.
NEWS RELEASES
CLICK HERE to read about Vistek in Quality Digest's article, "Controlling Electronic Records", September 2008 issue.
The article focuses on an in-depth case study involving Vistek Precision Machine Co. demonstrating how software helped a medical device manufacturer organize its systems in pursuit of ISO registration, maintain visibility over audits and cost tracking, and achieve FDA compliance.
The Vistek experience demonstrated that software integration and simplification streamlined the management of documents. Vince Visco, President of Vistek, reflected,“The software can associate a document to a training record and notify staff automatically,so we remain compliant."
Visco added, "This module helps us manage all aspects of our training requirements, and it captures the costs associated with training and the lack thereof. The days of the old paper training matrix have come to an end, further reducing our costs and satisfying the Part 11 requirement regarding trained and experienced personnel.”
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