# Anodyne Medical Device Inc. dba Tridien Medical, Coral Springs, FL – FDA Inspections

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

> Inspection records and compliance data for Anodyne Medical Device Inc. dba Tridien Medical in Coral Springs, Florida. 2 FDA inspections on record, last inspected August 13, 2015.

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## Details

- Name: Anodyne Medical Device Inc. dba Tridien Medical
- FEI Number: 1000222145
- Address Line 1: 4200 NW 120th Ave
- City: Coral Springs
- State: Florida
- Zip Code: 33065
- Country Name: United States
- Address: 4200 NW 120th Ave, Coral Springs, Florida 33065, United States
- Country: United States

## Related Documents

- [FDA Inspection 937282 - Anodyne Medical Device Inc. dba Tridien Medical - 2015-08-13](https://www.keypedia.com/records/fda_inspections/anodyne-medical-device-inc-dba-tridien-medical/7e6f7233-7817-4a67-b4cb-b92997de3170) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 13, 2015
- FDA Inspection 937282 - Anodyne Medical Device Inc. dba Tridien Medical - 2015-08-13 — classification: No Action Indicated (NAI), source: FDA, date: August 13, 2015
- [FDA Inspection 752929 - Anodyne Medical Device Inc. dba Tridien Medical - 2011-11-02](https://www.keypedia.com/records/fda_inspections/anodyne-medical-device-inc-dba-tridien-medical/f32e452d-70f2-4a25-ae55-414c33db85cb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 2, 2011
- FDA Inspection 752929 - Anodyne Medical Device Inc. dba Tridien Medical - 2011-11-02 — classification: No Action Indicated (NAI), source: FDA, date: November 2, 2011

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