# Adroit Medical Systems Inc - Inspection Records

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. Access full analysis and detailed observations.

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## Details

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

## Related Documents

- [FDA Inspection 1278307 - Adroit Medical Systems Inc - 2025-07-11](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/507b88de-31e8-4b62-8a76-5e5e51571de4) — source: FDA, date: July 11, 2025
- [FDA Inspection 1278307 - Adroit Medical Systems Inc - 2025-07-11](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/1445c2e9-6a99-4a3b-b9a7-447c3c29ab11) — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2025
- [FDA Inspection 1278307 - Adroit Medical Systems Inc - 2025-07-11](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/76a89126-e433-4e63-8f38-c10cf35cb73f) — 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](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/4a944ad2-90a9-4f7e-91df-53717200a376) — 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](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/9b23a5c2-4e0a-4645-b402-3589012d2f6b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 23, 2012
- [FDA Inspection 765950 - Adroit Medical Systems Inc - 2012-01-23](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/77f5379b-74ac-411a-840b-00f20820335f) — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2012
- [FDA Inspection 642668 - Adroit Medical Systems Inc - 2010-01-28](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/7ac91d77-e34a-4d4d-b46c-d5eb35a0f7cd) — classification: No Action Indicated (NAI), source: FDA, date: January 28, 2010

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