FDA Inspection 818779 — TYTEX SLOVAKIA S.R.O.
The FDA completed an inspection of TYTEX SLOVAKIA S.R.O. on January 24, 2013 in Humenne. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- January 24, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Humenne (Slovakia)