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FDA Inspection
•Kentron Health Care Inc•January 26, 2016

Kentron Health Care Inc – FDA Inspection, Jan 26, 2016

Record Details

This FDA Inspection record concerns Kentron Health Care Inc, with an inspection on January 26, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Kentron Health Care Inc
Inspection Date
January 26, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 76147c4b-696f-472d-b366-a3a22166baa2

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
956497
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

1
  1. 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Kentron Health Care Inc

4
DateClassificationOfficeProject area
February 5, 2020NAICenter for Devices and Radiological HealthCompliance: Devices
June 13, 2012NAICenter for Devices and Radiological HealthCompliance: Devices
October 12, 2011OAICenter for Devices and Radiological HealthCompliance: Devices
September 14, 2009NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Kentron Health Care Inc
  • FDA Inspection 1118867 - 2020-02-05
  • FDA Inspection 787821 - 2012-06-13
  • FDA Inspection 751028 - 2011-10-12
  • FDA Inspection 611888 - 2009-09-14

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