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Panel accuses FDA of dragging its feet
A congressional panel accuses the FDA of bureaucratic neglect in medical device regulation. The report faulted the agency for delayed enforcement since 1976, noting limited actions and few orders to repair or refund, while stressing the need for stronger safety oversight.
MENTIONED IN THIS ARTICLE
FDA
Washington
Food and Drug Administration
House Energy and Commerce Committee
Oversight and Investigations
John D. Dingell
Dmidh
Bill Grigg