# FDA Inspection 642668 - Adroit Medical Systems Inc - January 28, 2010

Source: https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/7ac91d77-e34a-4d4d-b46c-d5eb35a0f7cd
Source feed: FDA_Inspections

> FDA Inspection 642668 for Adroit Medical Systems Inc on January 28, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 642668
- Company Name: Adroit Medical Systems Inc
- Inspection Date: 2010-01-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1278307 - 2025-07-11](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/1445c2e9-6a99-4a3b-b9a7-447c3c29ab11)
- [FDA Inspection 1278307 - 2025-07-11](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/507b88de-31e8-4b62-8a76-5e5e51571de4)
- [FDA Inspection 1278307 - 2025-07-11](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/76a89126-e433-4e63-8f38-c10cf35cb73f)
- [FDA Inspection 1085944 - 2019-04-11](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/4a944ad2-90a9-4f7e-91df-53717200a376)
- [FDA Inspection 1085944 - 2019-04-11](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/4aac48a8-eef6-43d8-ae94-4ab3b15084fc)

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

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