FDA Inspection 859239 — Rudischhauser Surgical Instruments Manufacturing GmbH
The FDA completed an inspection of Rudischhauser Surgical Instruments Manufacturing GmbH on Dec 4, 2013 in Tuttlingen. 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 4, 2013
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Tuttlingen (Germany)