Always.
When it comes to the repair of medical equipment there is no room for error.
The servicing of life-saving medical devices requires precision, training, and accountability.
Patient safety demands that servicing of medical equipment be conducted by trained, authorized, and regulated servicers who are accountable to the U.S. Food and Drug Administration (FDA).
Our mission is simple:
Ensure those who service or repair medical technology used to treat or diagnose patients are qualified and follow FDA guidance.
Latest Newsroom
Any Federal Right to Repair Law Needs Medical Device Carve Outs
On Tuesday, the White House hosted a virtual briefing on right to repair highlighting the various federal and state actions aimed at giving consumers more control over…
How Cybersecurity Could be at Risk With Right to Repair
Conversations in state houses across the country are surfacing around right to repair. Just last month, California finalized their version of a right to repair bill that…
Former FDA Official Weighs in On Harms Associated with Medical Device Right to Repair
As the U.S. Copyright Office concludes its review of exemptions to Section 1201 of the Digital Millenium Copyright Act (DMCA), Peter Pitts, president of the Center for…
ACI Comments on Medical Device Exemptions Under DMCA
When Congress passed the Digital Millennium Copyright Act (DMCA) in 1998 they established a rulemaking process that gives the Library of Congress the power to make exceptions…
The Safe Repair Project is an initiative of The American Consumer Institute Center for Citizen Research, a 501(c)(3) nonprofit educational and research institute, whose core mission is to promote consumer welfare.