FDA Inspection 1027670 — Dreve Otoplastik Gmbh
The FDA completed an inspection of Dreve Otoplastik Gmbh on Sep 7, 2017 in Unna. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.
Inspection details
- Classification
- Official Action Indicated (OAI)
- End Date
- Sep 7, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Unna (Germany)