FDA Inspection
Fonar CorporationFonar Corporation – FDA Inspection, May 22, 2015
Record Details
This FDA Inspection record concerns Fonar Corporation, with an inspection on May 22, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Fonar Corporation
- Inspection Date
- May 22, 2015
- Product Type
- Devices
View Company Profile
ID · 926a4172-53be-4e13-9b2f-286fe85f23b6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 926699
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
FDA Citations
6- 21 CFR 820.70(f)Buildings
- 21 CFR 820.100(b)Documentation
- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.70(e)Contamination control, Lack of or inadequate procedures
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Other FDA inspections of Fonar Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| January 17, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 19, 2013 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| October 26, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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