# Adroit Medical Systems Inc, Loudon, TN – FDA Inspections

Source: https://www.keypedia.com/companies/adroit-medical-systems-inc/cb9c4b92-9482-4329-b9b4-823f58c7936c

> Inspection records and compliance data for Adroit Medical Systems Inc in Loudon, Tennessee. 5 FDA inspections on record, 2 Form 483s, last inspected July 11, 2025.

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## Details

- Name: Adroit Medical Systems Inc
- FEI Number: 1000111140
- Address Line 1: 1146 Carding Machine Rd
- City: Loudon
- State: Tennessee
- Zip Code: 37774
- Country Name: United States
- Address: 1146 Carding Machine Rd, Loudon, Tennessee 37774, United States
- Country: United States

## Related Documents

- FDA Inspection 1278307 - Adroit Medical Systems Inc - 2025-07-11 — source: FDA, date: July 11, 2025
- FDA Inspection 1278307 - Adroit Medical Systems Inc - 2025-07-11 — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2025
- FDA Inspection 1278307 - Adroit Medical Systems Inc - 2025-07-11 — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2025
- [FDA Inspection 1085944 - Adroit Medical Systems Inc - 2019-04-11](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/4aac48a8-eef6-43d8-ae94-4ab3b15084fc) — classification: No Action Indicated (NAI), source: FDA, date: April 11, 2019
- FDA Inspection 1085944 - Adroit Medical Systems Inc - 2019-04-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 11, 2019
- [FDA Inspection 1017646 - Adroit Medical Systems Inc - 2017-07-12](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/0a49925c-d027-450a-a454-1bba0f57c991) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 12, 2017
- FDA Inspection 765950 - Adroit Medical Systems Inc - 2012-01-23 — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2012
- FDA Inspection 765950 - Adroit Medical Systems Inc - 2012-01-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 23, 2012
- FDA Inspection 642668 - Adroit Medical Systems Inc - 2010-01-28 — classification: No Action Indicated (NAI), source: FDA, date: January 28, 2010

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