FDA Inspection
Tingle X-Ray Products IncTingle X-Ray Products Inc – FDA Inspection, Jun 23, 2017
Record Details
This FDA Inspection record concerns Tingle X-Ray Products Inc, with an inspection on June 23, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Wendy R. Blame (Issuing Officer)
View Company Profile
ID · 9de4dfcd-f74a-437f-ade0-7d6404d0fd09
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1018344
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Tingle X-Ray Products Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| July 17, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 22, 2013 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Tingle X-Ray Products Inc
- FDA Inspection 887526 - 2014-07-17
- FDA Inspection 823246 - 2013-03-22
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