FDA Inspection 898920 — ONTEX HYGIENEARTIKEL DEUTSCHLAND GMBH
The FDA completed an inspection of ONTEX HYGIENEARTIKEL DEUTSCHLAND GMBH on September 18, 2014 in Grosspostwitz/O.L.. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- September 18, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Grosspostwitz/O.L. (Germany)