# Michelson Diagnostics Ltd – FDA Inspection, Feb 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/michelson-diagnostics-ltd/30e5599c-0fa8-4934-83a7-b9e731dd4009
Source feed: FDA_Inspections

> FDA inspection 1005870 of Michelson Diagnostics Ltd, February 02, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1005870
- Company Name: Michelson Diagnostics Ltd
- Inspection Date: 2017-02-02
- 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: 0

## Related Documents

- [FDA Inspection 1226492 - 2023-12-13](https://www.keypedia.com/records/fda_inspections/michelson-diagnostics-ltd/ff5b81be-1c2d-4d1f-96ff-e30ab36958ab)

## Related Officers

- [Sean T. Creighton](https://www.keypedia.com/people/sean-t-creighton/80ffecab-0a2d-4727-a11f-407b697f4503)

Company: https://www.keypedia.com/companies/michelson-diagnostics-ltd/ec93b130-8bb8-466f-8a13-29553f46dce5

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