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FDA Inspection
•KMC Systems, Inc.•October 5, 2017

KMC Systems, Inc. – FDA Inspection, Oct 5, 2017

Record Details

This FDA Inspection record concerns KMC Systems, Inc., with an inspection on October 5, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
KMC Systems, Inc.
Inspection Date
October 5, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • James W. Whitney (Issuing Officer)
View Company Profile

ID · c639ee0e-36a2-4962-817e-47f6719ed4e6

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1028786
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of KMC Systems, Inc.

5
DateClassificationOfficeProject area
April 10, 2024NAICenter for Devices and Radiological HealthCompliance: Devices
August 18, 2021NAICenter for Devices and Radiological HealthBioresearch Monitoring
March 11, 2015NAICenter for Devices and Radiological HealthCompliance: Devices
February 20, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
October 1, 2010NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for KMC Systems, Inc.
  • FDA Inspection 1246379 - 2024-04-10
  • FDA Inspection 1155514 - 2021-08-18
  • FDA Inspection 921815 - 2015-03-11
  • FDA Inspection 819147 - 2013-02-20
  • FDA Inspection 683609 - 2010-10-01

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