FDA Inspection
Sanuwave IncSanuwave Inc – FDA Inspection, Dec 15, 2014
Record Details
This FDA Inspection record concerns Sanuwave Inc, with an inspection on December 15, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Sanuwave Inc
- Inspection Date
- December 15, 2014
- Product Type
- Devices
View Company Profile
ID · 75133e96-6c51-4f81-819d-4fdbcc5ee794
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 907399
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Sanuwave Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| January 10, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 17, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 6, 2011 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| October 19, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 10, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Sanuwave Inc
- FDA Inspection 1041626 - 2018-01-10
- FDA Inspection 962343 - 2016-02-17
- FDA Inspection 756365 - 2011-12-06
- FDA Inspection 750410 - 2011-10-19
- FDA Inspection 611061 - 2009-09-10
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