# Diomedics, Inc. – FDA Inspection, May 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/diomedics-inc/6e672ca1-2df6-43b2-9dfa-d4a55782cdb8
Source feed: FDA_Inspections

> FDA inspection 1017180 of Diomedics, Inc., May 19, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1017180
- Company Name: Diomedics, Inc.
- Inspection Date: 2017-05-19
- 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 806234 - 2012-11-06
- FDA Inspection 575786 - 2009-04-15

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/richard-k-vogel/3ddd8bff-24fd-40ee-b0a7-fb5333a520f5)

Company: https://www.keypedia.com/companies/diomedics-inc/4db3bfb8-f68e-4088-a80e-c086e2016745

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