# FDA Inspection 937282 - Anodyne Medical Device Inc. dba Tridien Medical - August 13, 2015

Source: https://www.keypedia.com/records/fda_inspections/anodyne-medical-device-inc-dba-tridien-medical/5f26e321-d1b6-4a62-a960-a70b442e55fa
Source feed: FDA_Inspections

> FDA Inspection 937282 for Anodyne Medical Device Inc. dba Tridien Medical on August 13, 2015. Classification: No Action Indicated (NAI).

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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: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 937282 - 2015-08-13](https://www.keypedia.com/records/fda_inspections/anodyne-medical-device-inc-dba-tridien-medical/7e6f7233-7817-4a67-b4cb-b92997de3170)
- [FDA Inspection 752929 - 2011-11-02](https://www.keypedia.com/records/fda_inspections/anodyne-medical-device-inc-dba-tridien-medical/862cd27c-dc7f-43b8-b560-a38aa39d88ac)
- [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