FDA Inspection 1250923 — Strub Medical GmbH & Co. KG
The FDA completed an inspection of Strub Medical GmbH & Co. KG on Sep 26, 2024 in Neuhausen Ob Eck. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Sep 26, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Neuhausen Ob Eck (Germany)