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Precision ADM, a contract manufacturer specializing in additive manufacturing (AM), is now registered in FDA’s Registration and Device Listing Database.
The designation confirms that Precision ADM meets standards set by FDA to manufacture medical devices.
“We’re very proud to be the only metal additive manufacturing service provider in Canada to hold ISO 13485 Certification and FDA establishment registration,” Chief Executive Officer Martin Petrak said in a press release. “This highlights our commitment to Quality Management Systems and to providing regulatory-approved devices to our clients.”
Along with AM, Precision ADM’s capabilities include subtractive multi-axis machining, design and testing services.
Source: Precision ADM
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