FDA Inspection 830498 — ONTEX HYGIENEARTIKEL DEUTSCHLAND GMBH
The FDA completed an inspection of ONTEX HYGIENEARTIKEL DEUTSCHLAND GMBH on April 11, 2013 in Grosspostwitz/O.L.. 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
- April 11, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Grosspostwitz/O.L. (Germany)