# Adroit Medical Systems Inc – FDA Inspection, Jul 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/0a49925c-d027-450a-a454-1bba0f57c991
Source feed: FDA_Inspections

> FDA inspection 1017646 of Adroit Medical Systems Inc, July 12, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1017646
- Company Name: Adroit Medical Systems Inc
- Inspection Date: 2017-07-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1278307 - 2025-07-11
- [FDA Inspection 1085944 - 2019-04-11](https://www.keypedia.com/records/fda_inspections/adroit-medical-systems-inc/4aac48a8-eef6-43d8-ae94-4ab3b15084fc)
- FDA Inspection 765950 - 2012-01-23
- FDA Inspection 642668 - 2010-01-28

## Related Officers

- Issuing Officer

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