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FDA Inspection
•Electrical Geodesics, Inc.•March 27, 2015

Electrical Geodesics, Inc. – FDA Inspection, Mar 27, 2015

Record Details

This FDA Inspection record concerns Electrical Geodesics, Inc., with an inspection on March 27, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company
Electrical Geodesics, Inc.
Inspection Date
March 27, 2015
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · c14dba49-8adb-45d5-9505-fa8bfd24c390

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
920345
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

2
  1. 21 CFR 820.184DHR - not or inadequately maintained
  2. 21 CFR 820.181DMR - not or inadequately maintained

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Electrical Geodesics, Inc.

3
DateClassificationOfficeProject area
June 17, 2016VAICenter for Devices and Radiological HealthBioresearch Monitoring
August 12, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
August 12, 2010NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Electrical Geodesics, Inc.
  • FDA Inspection 978919 - 2016-06-17
  • FDA Inspection 674766 - 2010-08-12
  • FDA Inspection 674765 - 2010-08-12

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