Home » Devicemakers Should Focus on Resolution, Not Number, of CAPA Files: CDRH Official
Devicemakers Should Focus on Resolution, Not Number, of CAPA Files: CDRH Official
Devicemakers should never be concerned that an FDA inspector will cite them for opening “too many” corrective and preventative actions, a CDRH official says.
Devices & Diagnostics Letter
Devices Inspections and AuditsDevices & Diagnostics Letter
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