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FDA Inspection
•Hema Diagnostic Systems, L.L.C.•December 10, 2014

Hema Diagnostic Systems, L.L.C. – FDA Inspection, Dec 10, 2014

Record Details

This FDA Inspection record concerns Hema Diagnostic Systems, L.L.C., with an inspection on December 10, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company
Hema Diagnostic Systems, L.L.C.
Inspection Date
December 10, 2014
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 597c5268-4965-4ff7-b0c3-dc49d6123f74

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
909107
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Hema Diagnostic Systems, L.L.C.

1
DateClassificationOfficeProject area
March 11, 2013OAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Hema Diagnostic Systems, L.L.C.
  • FDA Inspection 821895 - 2013-03-11

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