# FDA Inspection 818779 - TYTEX SLOVAKIA S.R.O. - January 24, 2013

Source: https://www.keypedia.com/records/fda_inspections/tytex-slovakia-sro/09a5451d-7664-4c2e-a81d-4b1de7bc22a0
Source feed: FDA_Inspections

> FDA Inspection 818779 for TYTEX SLOVAKIA S.R.O. on January 24, 2013. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 818779
- Company Name: TYTEX SLOVAKIA S.R.O.
- Inspection Date: 2013-01-24
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/tytex-slovakia-sro/88bada4f-f1ed-44bd-8509-19c2d8cef543

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