# Anodyne Medical Device Inc. dba Tridien Medical – FDA Inspection, Aug 13, 2015

Source: https://www.keypedia.com/records/fda_inspections/anodyne-medical-device-inc-dba-tridien-medical/7e6f7233-7817-4a67-b4cb-b92997de3170
Source feed: FDA_Inspections

> FDA inspection 937282 of Anodyne Medical Device Inc. dba Tridien Medical, August 13, 2015. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 937282
- Company Name: Anodyne Medical Device Inc. dba Tridien Medical
- Inspection Date: 2015-08-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 752929 - 2011-11-02](https://www.keypedia.com/records/fda_inspections/anodyne-medical-device-inc-dba-tridien-medical/f32e452d-70f2-4a25-ae55-414c33db85cb)

Company: https://www.keypedia.com/companies/anodyne-medical-device-inc-dba-tridien-medical/bb068b50-c9e8-4a1e-b372-710960d38e37

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7