FDA Inspection
TIDI Products, LLCTIDI Products, LLC – FDA Inspection, May 30, 2018
Record Details
This FDA Inspection record concerns TIDI Products, LLC, with an inspection on May 30, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · a89b5710-367a-47be-a726-535eb8b60621
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1055339
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of TIDI Products, LLC
4| Date | Classification | Office | Project area |
|---|---|---|---|
| December 9, 2021 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 25, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 15, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 6, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for TIDI Products, LLC
- FDA Inspection 1161536 - 2021-12-09
- FDA Inspection 885452 - 2014-06-25
- FDA Inspection 681404 - 2010-09-15
- FDA Inspection 656041 - 2010-04-06
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