FDA

Myriad is registered with the FDA as a Contract Device Manufacturer. Our registration Number is available upon request. Our facility is cGMP compliant under 21CFR 820.

ISO

Myriad is also ISO 13485:2003 certified, as a contract manufacturer of fiber optic imaging and illumination devices for the medical device industry. This certificate also covers our machine shop services.

Myriad's quality system has been audited and found compliant to; ISO 9001, and the Japanese standard: MHLW Ministerial Ordinance No. 169, 2004.

 

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OUR COMMITMENT:

To meet or exceed our customer's specifications when developing and manufacturing products.

 

OUR QUALITY:

Is built into each product by skilled team members and proudly delivered to our customers.