TYTEX SLOVAKIA S.R.O. – FDA Inspection, Jan 24, 2013

Record Details

This FDA Inspection record concerns TYTEX SLOVAKIA S.R.O., with an inspection on January 24, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: TYTEX SLOVAKIA S.R.O.
Inspection Date: January 24, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 09a5451d-7664-4c2e-a81d-4b1de7bc22a0

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number: 818779
FDA center: Medical Devices & Rad Health
Project area: Compliance: Devices

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FDA Inspection

TYTEX SLOVAKIA S.R.O.January 24, 2013