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Orchid Keller
Quality
Quality has been at the foundation of Keller Engineering since it was founded in 1972. When medical device manufacturing moved to
the forefront of Keller's business in 1998, this tradition of quality throughout the organization proved to be a key component of
our success. "When we manufacture something for bio-compatibility, something that is used inside the human body, there is no room
for error," explains Vice President and General Manager Steve Dragovich. "Because these parts must be perfect, each manufacturing
operation at Keller is scrutinized to assure the quality of everything we make."
ISO 9002 Compliant ISO 13485 Certification in Process
FDA Registered Compliant with GMP Standards
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