FDA Inspection
Anodyne Medical Device Inc. dba Tridien MedicalAnodyne Medical Device Inc. dba Tridien Medical – FDA Inspection, Aug 13, 2015
Record Details
This FDA Inspection record concerns Anodyne Medical Device Inc. dba Tridien Medical, with an inspection on August 13, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- August 13, 2015
- Product Type
- Devices
View Company Profile
ID · 7e6f7233-7817-4a67-b4cb-b92997de3170
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 937282
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Anodyne Medical Device Inc. dba Tridien Medical
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 2, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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