# Arc Devices USA Inc – FDA Inspection, Aug 31, 2018

Source: https://www.keypedia.com/records/fda_inspections/arc-devices-usa-inc/c05eae90-6216-4995-a340-683c41d3109f
Source feed: FDA_Inspections

> FDA inspection 1065455 of Arc Devices USA Inc, August 31, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1065455
- Company Name: Arc Devices USA Inc
- Inspection Date: 2018-08-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [Investigator](https://www.keypedia.com/people/david-m-wilkinson/5e81ba03-7602-46d6-b675-26efc77d28db)

Company: https://www.keypedia.com/companies/arc-devices-usa-inc/0f520687-fdb6-4ace-9367-9bce625fe02d

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