# FDA Inspection 1017180 - Diomedics, Inc. - 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 for Diomedics, Inc. on May 19, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1017180
- Company Name: Diomedics, Inc.
- Inspection Date: 2017-05-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1017180 - 2017-05-19](https://www.keypedia.com/records/fda_inspections/diomedics-inc/3d1d5baa-f3bb-4df0-838c-116cb49d7fb8)
- [FDA Inspection 806234 - 2012-11-06](https://www.keypedia.com/records/fda_inspections/diomedics-inc/0c18ba62-c5bc-4ab3-aea0-2abd7a8ebb40)
- [FDA Inspection 806234 - 2012-11-06](https://www.keypedia.com/records/fda_inspections/diomedics-inc/54968398-3912-46e8-bba8-aaf7bd019b75)
- [FDA Inspection 575786 - 2009-04-15](https://www.keypedia.com/records/fda_inspections/diomedics-inc/a8156969-3fd2-4f4c-99a1-afc845cf5675)
- [FDA Inspection 575786 - 2009-04-15](https://www.keypedia.com/records/fda_inspections/diomedics-inc/bbc45007-1f8e-426e-8b46-3f0a441419ed)

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