# EDM3 LLC – FDA Inspection, Jun 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/edm3-llc/f1aff385-8e64-42b8-b84e-6e71d98851bf
Source feed: FDA_Inspections

> FDA inspection 1016612 of EDM3 LLC, June 30, 2017. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016612
- Company Name: EDM3 LLC
- Inspection Date: 2017-06-30
- 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: 6

## Related Documents

- FDA Inspection 879443 - 2014-05-12
- FDA Inspection 767068 - 2012-02-06

## Related Officers

- [Joshua J. Silvestri](https://www.keypedia.com/people/joshua-j-silvestri/433e29b3-ce5f-44d2-9984-7a6cb61e1824)

Company: https://www.keypedia.com/companies/edm3-llc/ab044c7c-bca0-4398-a96c-c0f4e3584233

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