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FDA Inspection
•Cenogenics Corporation•October 17, 2017

Cenogenics Corporation – FDA Inspection, Oct 17, 2017

Record Details

This FDA Inspection record concerns Cenogenics Corporation, with an inspection on October 17, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Cenogenics Corporation
Inspection Date
October 17, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Gobiga Vanniyasingam (Company Rep)
View Company Profile

ID · 9269389f-df1e-4e8a-8556-abdfb97f3ccc

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1028854
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 820.100(b)Documentation
  2. 21 CFR 820.184DHR content
  3. 21 CFR 820.198(e)Records of complaint investigation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Cenogenics Corporation

4
DateClassificationOfficeProject area
February 5, 2026Not classifiedNew Jersey District Office
June 12, 2023NAICenter for Devices and Radiological HealthCompliance: Devices
June 16, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
May 18, 2009NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Cenogenics Corporation
  • FDA Inspection 1302632 - 2026-02-05
  • FDA Inspection 1208548 - 2023-06-12
  • FDA Inspection 729965 - 2011-06-16
  • FDA Inspection 583265 - 2009-05-18

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