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FDA Inspection
•Fonar Corporation•April 19, 2013

Fonar Corporation – FDA Inspection, Apr 19, 2013

Record Details

This FDA Inspection record concerns Fonar Corporation, with an inspection on April 19, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Fonar Corporation
Inspection Date
April 19, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 939c7b90-fb33-42da-81b0-6b1e406dd0be

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
828379
FDA center
Medical Devices & Rad Health
Project area
Radiation Control and Health Safety Act

FDA Citations

3
  1. 21 CFR 820.198(a)Complaints
  2. 21 CFR 820.100(b)Documentation
  3. 21 CFR 820.40(a)Document review, approval documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Fonar Corporation

3
DateClassificationOfficeProject area
January 17, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
May 22, 2015VAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
October 26, 2010VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Fonar Corporation
  • FDA Inspection 997473 - 2017-01-17
  • FDA Inspection 926699 - 2015-05-22
  • FDA Inspection 700585 - 2010-10-26

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