# Dewan Asheesh – FDA Inspection, Mar 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/dewan-asheesh/b029cae4-e79b-4a21-9f4e-130d3d6d949c
Source feed: FDA_Inspections

> FDA inspection 1006851 of Dewan Asheesh, March 13, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1006851
- Company Name: Dewan Asheesh
- Inspection Date: 2017-03-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [Company Rep](https://www.keypedia.com/people/rebecca-t-davis/a821f7ef-0c73-4be1-9a9b-3fc2c07f88c1)

Company: https://www.keypedia.com/companies/dewan-asheesh/23ef6bf5-1ee7-4928-909a-223ce13f2179

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