FDA Inspection 1061002 — ONTEX HYGIENEARTIKEL DEUTSCHLAND GMBH
The FDA completed an inspection of ONTEX HYGIENEARTIKEL DEUTSCHLAND GMBH on June 21, 2018 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
- June 21, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Grosspostwitz/O.L. (Germany)