FDA Inspection
PainDx, Inc.PainDx, Inc. – FDA Inspection, Jan 23, 2020
Record Details
This FDA Inspection record concerns PainDx, Inc., with an inspection on January 23, 2020, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- PainDx, Inc.
- Inspection Date
- January 23, 2020
- Product Type
- Devices
View Company Profile
ID · 209ed068-7a89-40bb-89ac-c1c1126bc96d
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1118743
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of PainDx, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| January 19, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 8, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 5, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 11, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for PainDx, Inc.
- FDA Inspection 1195462 - 2023-01-19
- FDA Inspection 984449 - 2016-06-08
- FDA Inspection 868638 - 2014-03-05
- FDA Inspection 647131 - 2010-02-11
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