# LM-Instruments Oy – FDA Inspection, May 31, 2018

Source: https://www.keypedia.com/records/fda_inspections/lm-instruments-oy/1d4544d6-d25c-421f-9d58-5fdc75bf1537
Source feed: FDA_Inspections

> FDA inspection 1054117 of LM-Instruments Oy, May 31, 2018. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803, 806 and 820. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1054117
- Company Name: LM-Instruments Oy
- Inspection Date: 2018-05-31
- 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 Officers

- [Investigator](https://www.keypedia.com/people/akbar-j-zaidi/9cd9ac91-2d4b-4f6f-a975-865342075924)

Company: https://www.keypedia.com/companies/lm-instruments-oy/42929e9e-e54b-4a80-a23d-8da1f195a8e5

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