# Belimed D.O.O. – FDA Inspection, Jun 21, 2019

Source: https://www.keypedia.com/records/fda_inspections/belimed-doo/a2b07fdd-da07-42a9-9a54-d2e36c836fb9
Source feed: FDA_Inspections

> FDA inspection 1094102 of Belimed D.O.O., June 21, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1094102
- Company Name: Belimed D.O.O.
- Inspection Date: 2019-06-21
- 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 Officers

- [FDA Associated Person](https://www.keypedia.com/people/joseph-r-strelnik/1fb7d50e-abf2-45ef-85a8-71c61b33e42d)

Company: https://www.keypedia.com/companies/belimed-doo/197e1323-a51c-4710-a4bb-02144b41050a

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