FDA Inspection 1082136 — OEHM UND REHBEIN GMBH
The FDA completed an inspection of OEHM UND REHBEIN GMBH on Jan 17, 2019 in Rostock. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jan 17, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Rostock (Germany)