# SEISA EUROPE S.R.O. – FDA Inspection, Jun 20, 2012

Source: https://www.keypedia.com/records/fda_inspections/seisa-europe-sro/0cca0ef1-10e7-4d46-8378-8735b4cdc954
Source feed: FDA_Inspections

> FDA inspection 792437 of SEISA EUROPE S.R.O., June 20, 2012. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 792437
- Company Name: SEISA EUROPE S.R.O.
- Inspection Date: 2012-06-20
- 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: 1

Company: https://www.keypedia.com/companies/seisa-europe-sro/4a6c39c4-ece1-4ff6-9e91-26dc77406a6b

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