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FDA Inspection
•Epigenomics Ag•June 29, 2017

Epigenomics Ag – FDA Inspection, Jun 29, 2017

Record Details

This FDA Inspection record concerns Epigenomics Ag, with an inspection on June 29, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Epigenomics Ag
Inspection Date
June 29, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Richard K. Vogel (FDA Associated Person)
View Company Profile

ID · f79a5f7a-0c45-4377-9ba0-58ff96090833

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1017636
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Epigenomics Ag

2
DateClassificationOfficeProject area
June 18, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 24, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Epigenomics Ag
  • FDA Inspection 931087 - 2015-06-18
  • FDA Inspection 833099 - 2013-05-24

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