FDA Inspection 939718 — Hasomed GmbH
The FDA completed an inspection of Hasomed GmbH on Jun 25, 2015 in Magdeburg. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jun 25, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Magdeburg (Germany)