S 3395
Medical Device Integrity Act
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Sign in to take action- Introduced
- Passed Senate
- Passed House
- To President
- Became Law
Bill overview
Medical Device Integrity Act This bill provides the Food and Drug Administration (FDA) with the authority to request records and information from an establishment that manufactures or otherwise prepares medical devices. Currently, the FDA only has statutory authority to make such requests to establishments that manufacture or otherwise prepare drugs. The bill also requires the FDA to include in its requests a rationale for requesting the information in question.
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Primary sponsor
Cosponsors
Robert P., Jr. Casey
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