# EKOM spol. s.r.o. – FDA Inspection, Oct 25, 2012

Source: https://www.keypedia.com/records/fda_inspections/ekom-spol-sro/f2f611df-24e4-413a-a068-f976bd802cf2
Source feed: FDA_Inspections

> FDA inspection 811214 of EKOM spol. s.r.o., October 25, 2012. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 811214
- Company Name: EKOM spol. s.r.o.
- Inspection Date: 2012-10-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1319224 - 2026-05-28](https://www.keypedia.com/records/fda_inspections/ekom-spol-sro/e5f8c409-be32-45f1-bb82-fbe315c36c38)
- [FDA Inspection 1233666 - 2024-03-21](https://www.keypedia.com/records/fda_inspections/ekom-spol-sro/fd9e3c38-38cc-4063-bcec-94be8a40b1ec)
- FDA Inspection 1016985 - 2017-05-25

Company: https://www.keypedia.com/companies/ekom-spol-sro/2313a8b1-5ab5-44e9-bd98-9550e47e61eb

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