FDA Inspection 859242 — Rominger Medizintechnik GmbH
The FDA completed an inspection of Rominger Medizintechnik GmbH on Dec 11, 2013 in Seitingen-Oberflacht. 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
- Dec 11, 2013
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Seitingen-Oberflacht (Germany)