# Diatron MI Plc – FDA Inspection, Feb 9, 2023

Source: https://www.keypedia.com/records/fda_inspections/diatron-mi-plc/e801d798-ba38-4dab-a42e-b48d02add113
Source feed: FDA_Inspections

> FDA inspection 1197444 of Diatron MI Plc, February 09, 2023. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1197444
- Company Name: Diatron MI Plc
- Inspection Date: 2023-02-09
- 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: 6

## Related Documents

- FDA Inspection 1301970 - 2025-11-20
- [FDA Inspection 1012057 - 2017-05-19](https://www.keypedia.com/records/fda_inspections/diatron-mi-plc/3a18fb13-b0dd-4329-943d-b7cd1635a6ca)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/christine-i-shaw/480cb61e-f173-432d-b84a-c8b492192302)

Company: https://www.keypedia.com/companies/diatron-mi-plc/99657ad1-d752-4e22-b69e-9d36748d50d5

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