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FDA Inspection
•CareHealth America DBA Express Diagnostics International•October 29, 2008

CareHealth America DBA Express Diagnostics International – FDA Inspection, Oct 29, 2008

Record Details

This FDA Inspection record concerns CareHealth America DBA Express Diagnostics International, with an inspection on October 29, 2008, issued by the Center for Devices and Radiological Health, covering devices.

Company
CareHealth America DBA Express Diagnostics International
Inspection Date
October 29, 2008
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 5c3ee50b-1797-4e00-931f-9ef9ff19f16c

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
543591
FDA center
Medical Devices & Rad Health
Project area
Bioresearch Monitoring

Other FDA inspections of CareHealth America DBA Express Diagnostics International

5
DateClassificationOfficeProject area
January 25, 2024NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
September 25, 2015NAICenter for Devices and Radiological HealthCompliance: Devices
June 24, 2014OAICenter for Devices and Radiological HealthCompliance: Devices
July 13, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
January 20, 2011OAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for CareHealth America DBA Express Diagnostics International
  • FDA Inspection 1229070 - 2024-01-25
  • FDA Inspection 949582 - 2015-09-25
  • FDA Inspection 883813 - 2014-06-24
  • FDA Inspection 734603 - 2011-07-13
  • FDA Inspection 706649 - 2011-01-20

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