# Medi-Globe s.r.o. – FDA Inspection, Oct 22, 2010

Source: https://www.keypedia.com/records/fda_inspections/medi-globe-sro/2b58a826-0826-43d5-87fd-172a261f9cd2
Source feed: FDA_Inspections

> FDA inspection 699088 of Medi-Globe s.r.o., October 22, 2010. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 699088
- Company Name: Medi-Globe s.r.o.
- Inspection Date: 2010-10-22
- 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: 4

## Related Documents

- [FDA Inspection 1055265 - 2018-05-24](https://www.keypedia.com/records/fda_inspections/medi-globe-sro/99649e38-d74b-4051-bc24-359f23214ccc)
- [FDA Inspection 917429 - 2015-02-20](https://www.keypedia.com/records/fda_inspections/medi-globe-sro/001c2447-e6d8-4d81-ad04-b8ff13158484)

Company: https://www.keypedia.com/companies/medi-globe-sro/933c5ac6-eb42-4ad3-8e19-3b9109a25d1f

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